SNP Report

Basic Info

Name	rs10997868 dbSNP Ensembl
Location	chr10:67905202 - 67905202(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.324681
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000212015, ENST00000406900, ENST00000432464, ENST00000473922); non_coding_transcript_variant(ENST00000473922); upstream_gene_variant(ENST00000403579)
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)
SIRT1	sirtuin 1	10q21	1(0/1/0)

SNPs in LD with rs10997868 (count: 0) View in gBrowse (chr10:67905202..67905202 )

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

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