SNP Report

Basic Info

Name	rs7098825 dbSNP Ensembl
Location	chr10:102868477 - 102868477(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.169329
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000339834, ENST00000369883); intron_variant(ENST00000299353); NMD_transcript_variant(ENST00000299353); non_coding_transcript_exon_variant(ENST00000636230); non_coding_transcript_variant(ENST00000636230); upstream_gene_variant(ENST00000369880, ENST00000615257)
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 rs7098825 (count: 0) View in gBrowse (chr10:102868477..102868477 )

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

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