SNP Report

Basic Info
Name rs10917671 dbSNP Ensembl
Location chr1:163069063 - 163069063(1)
Variant Alleles G/A
Ancestral Allele A
Minor Allele A
Minor Allele Frequence 0.455671
Functional Annotation intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000421743, ENST00000527393); non_coding_transcript_variant(ENST00000527393); upstream_gene_variant(ENST00000367906, ENST00000367908, ENST00000367909, ENST00000491263, ENST00000527809, ENST00000528938, ENST00000531057, ENST00000533019)
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)
RGS4 regulator of G-protein signaling 4 1q23.3 6(3/2/1)

SNPs in LD with rs10917671 (count: 0) View in gBrowse (chr1:163069063..163069063 )

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

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