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)