SNP Report

Basic Info

Name	rs2516482 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31519541 - 31519541(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.0910543
Functional Annotation	5_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000376191); downstream_gene_variant(ENST00000376177, ENST00000376185, ENST00000396172, ENST00000416625, ENST00000417023, ENST00000427214, ENST00000431908, ENST00000458640, ENST00000462256, ENST00000462421, ENST00000474961, ENST00000478365, ENST00000481456, ENST00000482195, ENST00000484566, ENST00000424816, ENST00000412386, ENST00000416325, ENST00000420337, ENST00000426766, ENST00000432549, ENST00000437943, ENST00000448800, ENST00000450413, ENST00000460622, ENST00000462334, ENST00000463430, ENST00000467581, ENST00000471062, ENST00000487410, ENST00000493350, ENST00000421209, ENST00000412106, ENST00000415689, ENST00000417590, ENST00000422243, ENST00000427425, ENST00000438449, ENST00000438578, ENST00000456476, ENST00000464411, ENST00000467694, ENST00000472840, ENST00000482077, ENST00000485571, ENST00000494127, ENST00000452195, ENST00000415390, ENST00000417558, ENST00000417995, ENST00000441425, ENST00000453138, ENST00000453488, ENST00000456043, ENST00000456666, ENST00000461254, ENST00000465849, ENST00000478906, ENST00000483957, ENST00000488094, ENST00000491058, ENST00000497007, ENST00000443405, ENST00000412330, ENST00000419391, ENST00000433293, ENST00000445218, ENST00000446341, ENST00000448000, ENST00000448296, ENST00000455916, ENST00000465854, ENST00000467175, ENST00000472906, ENST00000473685, ENST00000484344, ENST00000489325, ENST00000490964, ENST00000430073, ENST00000413678, ENST00000414088, ENST00000414440, ENST00000416863, ENST00000428107, ENST00000430703, ENST00000451666, ENST00000452792, ENST00000460187, ENST00000461080, ENST00000468089, ENST00000479206, ENST00000482080, ENST00000494457, ENST00000494835, ENST00000383512, ENST00000383508, ENST00000400293, ENST00000400295, ENST00000400296, ENST00000435182, ENST00000445602, ENST00000446328, ENST00000457032, ENST00000460555, ENST00000462954, ENST00000465016, ENST00000485534, ENST00000495391, ENST00000495997, ENST00000422733, ENST00000427489, ENST00000430784, ENST00000431360, ENST00000439927, ENST00000445480, ENST00000450987, ENST00000453381, ENST00000455400, ENST00000460280, ENST00000470514, ENST00000487541, ENST00000489688, ENST00000490297, ENST00000493860, ENST00000496801)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DDX39B	DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B	6p21.33	Mapped by LD-proxy
ATP6V1G2-DDX39B	ATP6V1G2-DDX39B readthrough (NMD candidate)	6p21.33	Mapped by LD-proxy

SNPs in LD with rs2516482 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31519541..31519541 )

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

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