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)