SNP Report

Basic Info

Name	rs3094005 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31488030 - 31488030(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.0648962
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000538442); upstream_gene_variant(ENST00000252229, ENST00000383850, ENST00000399150, ENST00000619506, ENST00000442104, ENST00000451603, ENST00000578117, ENST00000438954, ENST00000458032, ENST00000577383, ENST00000383514, ENST00000437651, ENST00000581780, ENST00000436531, ENST00000436655, ENST00000578893, ENST00000400313, ENST00000428416, ENST00000582440, ENST00000443156, ENST00000451789, ENST00000579799)
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)
MICB	MHC class I polypeptide-related sequence B	6p21.3	Mapped by LD-proxy

SNPs in LD with rs3094005 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31488030..31488030 )

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

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