SNP Report

Basic Info

Name	rs11191425 dbSNP Ensembl
Location	chr10:102866213 - 102866213(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.16274
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000339834, ENST00000369883); intron_variant(ENST00000299353); NMD_transcript_variant(ENST00000299353); upstream_gene_variant(ENST00000369880, ENST00000615257, ENST00000636230)
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)
C10orf32	chromosome 10 open reading frame 32	10q24.33	Mapped by LD-proxy
AS3MT	arsenite methyltransferase	10q24.33	1(1/0/0)

SNPs in LD with rs11191425 (count: 0) View in gBrowse (chr10:102866213..102866213 )

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

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