SNP Report

Basic Info

Name	rs6950845 dbSNP Ensembl
Location	chr7:7645426 - 7645426(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.218051
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000223129, ENST00000463725, ENST00000469183, ENST00000471760, ENST00000482067, ENST00000493246, ENST00000636849); non_coding_transcript_variant(ENST00000469183, ENST00000471760, ENST00000493246); upstream_gene_variant(ENST00000396682, ENST00000406109, ENST00000462723, ENST00000463632)
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)
RPA3-AS1	UBAP1-MVB12-associated (UMA) domain containing 1	7p21.3	Mapped by Literature SNP
RPA3	replication protein A3, 14kDa	7p21.3	1(1/0/0)

SNPs in LD with rs6950845 (count: 0) View in gBrowse (chr7:7645426..7645426 )

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

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