SNP Report

Basic Info

Name	rs3130614 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31499428 - 31499428(1)
Variant Alleles	T/A
Ancestral Allele	T
Minor Allele	A
Minor Allele Frequence	0.0259585
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000494577); intron_variant(ENST00000252229, ENST00000399150, ENST00000538442, ENST00000472772, ENST00000442104, ENST00000451603, ENST00000619506, ENST00000469155, ENST00000438954, ENST00000458032, ENST00000481200, ENST00000383514, ENST00000437651, ENST00000490718, ENST00000428059, ENST00000456351, ENST00000614843, ENST00000470406, ENST00000436531, ENST00000436655, ENST00000477414, ENST00000400313, ENST00000428416, ENST00000489566, ENST00000443156, ENST00000451789)
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 rs3130614 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31499428..31499428 )

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

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