SNP Report

Basic Info

Name	rs9267659 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31871144 - 31871144(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.127995
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000375528, ENST00000375530, ENST00000375537, ENST00000395728, ENST00000461880, ENST00000478491, ENST00000480912, ENST00000494816); intron_variant(ENST00000229729, ENST00000375562, ENST00000414427, ENST00000462671, ENST00000465707); non_coding_transcript_variant(ENST00000462671, ENST00000465707); upstream_gene_variant(ENST00000544672, ENST00000415323, ENST00000421926, ENST00000440987, ENST00000450323, ENST00000488695, ENST00000495638, ENST00000495740, ENST00000498185, ENST00000414684, ENST00000417894, ENST00000473048, ENST00000492911, ENST00000550401, ENST00000473048, ENST00000492911, ENST00000550821, ENST00000420874, ENST00000436403, ENST00000443951, ENST00000450075, ENST00000477385, ENST00000479567, ENST00000481372, ENST00000497104, ENST00000433046, ENST00000453831, ENST00000482758, ENST00000495620, ENST00000551168, ENST00000482758, ENST00000495620, ENST00000546461, ENST00000420930, ENST00000428442, ENST00000429506, ENST00000450229, ENST00000469160, ENST00000471633, ENST00000478077, ENST00000497361, ENST00000425238, ENST00000431710, ENST00000469478, ENST00000477158, ENST00000549663, ENST00000469478, ENST00000477158, ENST00000548188, ENST00000420336, ENST00000427405, ENST00000446303, ENST00000454705, ENST00000467139, ENST00000478205, ENST00000478629, ENST00000495830, ENST00000415517, ENST00000441920, ENST00000463111, ENST00000485731, ENST00000547493, ENST00000463111, ENST00000485731, ENST00000547288, ENST00000383372, ENST00000383373, ENST00000400006, ENST00000400008, ENST00000465456, ENST00000466693, ENST00000469681, ENST00000470058, ENST00000383379, ENST00000458130, ENST00000487790, ENST00000489833, ENST00000497745, ENST00000549677, ENST00000487790, ENST00000489833, ENST00000497745, ENST00000547684, ENST00000425250, ENST00000458593, ENST00000465316, ENST00000465622, ENST00000479426, ENST00000487513, ENST00000627114, ENST00000629838, ENST00000442152, ENST00000450933, ENST00000467209, ENST00000495181, ENST00000553121, ENST00000467209, ENST00000495181, ENST00000553147)
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)
EHMT2	euchromatic histone-lysine N-methyltransferase 2	6p21.3	Mapped by Literature SNP
SLC44A4	solute carrier family 44, member 4	6p21.3	Mapped by Literature SNP

SNPs in LD with rs9267659 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31871144..31871144 )

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

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