SNP Report

Basic Info

Name	rs2844463 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31638138 - 31638138(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.283347
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000424176, ENST00000424480, ENST00000428326, ENST00000433828, ENST00000434444, ENST00000441054, ENST00000451898, ENST00000452994, ENST00000454165, ENST00000456286, ENST00000456622); intron_variant(ENST00000211379, ENST00000362049, ENST00000375964, ENST00000375976, ENST00000435080, ENST00000437771, ENST00000439687); upstream_gene_variant(ENST00000438149, ENST00000453833, ENST00000462682, ENST00000465348, ENST00000469182, ENST00000470875, ENST00000416797, ENST00000421106, ENST00000422860, ENST00000425373, ENST00000429956, ENST00000438112, ENST00000440499, ENST00000441994, ENST00000442698, ENST00000444557, ENST00000447798, ENST00000453763, ENST00000459770, ENST00000482550, ENST00000417144, ENST00000421354, ENST00000425568, ENST00000442479, ENST00000449450, ENST00000551350, ENST00000615143, ENST00000445519, ENST00000455101, ENST00000456828, ENST00000488938, ENST00000493297, ENST00000494220, ENST00000497694, ENST00000416755, ENST00000420075, ENST00000420098, ENST00000428271, ENST00000431345, ENST00000431989, ENST00000432174, ENST00000436859, ENST00000438330, ENST00000446133, ENST00000452627, ENST00000456223, ENST00000466934, ENST00000483830, ENST00000415170, ENST00000422756, ENST00000425649, ENST00000434446, ENST00000449874, ENST00000552467, ENST00000613474, ENST00000419635, ENST00000435543, ENST00000455689, ENST00000463220, ENST00000488142, ENST00000491914, ENST00000497585, ENST00000415770, ENST00000416094, ENST00000419409, ENST00000424221, ENST00000427244, ENST00000427281, ENST00000428905, ENST00000432814, ENST00000436434, ENST00000441898, ENST00000450513, ENST00000454248, ENST00000461174, ENST00000462603, ENST00000415345, ENST00000415373, ENST00000444402, ENST00000447656, ENST00000451042, ENST00000550393, ENST00000615224, ENST00000432674, ENST00000436814, ENST00000451948, ENST00000461560, ENST00000461852, ENST00000472751, ENST00000478374, ENST00000416852, ENST00000420942, ENST00000430999, ENST00000433146, ENST00000435066, ENST00000438546, ENST00000438842, ENST00000448278, ENST00000453036, ENST00000453772, ENST00000453928, ENST00000456067, ENST00000480345, ENST00000497009, ENST00000412012, ENST00000413922, ENST00000438641, ENST00000442870, ENST00000454478, ENST00000546462, ENST00000621056, ENST00000413373, ENST00000439917, ENST00000445869, ENST00000460147, ENST00000476526, ENST00000484443, ENST00000497114, ENST00000412992, ENST00000414208, ENST00000415034, ENST00000417419, ENST00000421991, ENST00000424003, ENST00000431049, ENST00000436807, ENST00000442112, ENST00000446325, ENST00000451534, ENST00000455409, ENST00000474730, ENST00000483008, ENST00000361076, ENST00000383446, ENST00000383448, ENST00000418840, ENST00000432539, ENST00000552605, ENST00000617635, ENST00000417468, ENST00000431516, ENST00000453241, ENST00000471376, ENST00000476290, ENST00000478533, ENST00000482329, ENST00000417824, ENST00000426331, ENST00000433726, ENST00000434880, ENST00000436497, ENST00000437054, ENST00000437731, ENST00000437735, ENST00000439612, ENST00000442427, ENST00000449173, ENST00000458287, ENST00000462709, ENST00000471124, ENST00000419847, ENST00000428037, ENST00000436569, ENST00000443182, ENST00000451932, ENST00000552116, ENST00000615725, ENST00000411914, ENST00000423612, ENST00000429830, ENST00000460429, ENST00000469288, ENST00000485152, ENST00000496240)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
BAG6	BCL2-associated athanogene 6	6p21.3	Mapped by LD-proxy

SNPs in LD with rs2844463 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31638138..31638138 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)