SNP Report

Basic Info

Name	rs6785549 dbSNP Ensembl
Location	chr3:49699132 - 49699132(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.415335
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000443204, ENST00000454491, ENST00000629802); intron_variant(ENST00000327697, ENST00000432042, ENST00000457726, ENST00000486102, ENST00000487805); NMD_transcript_variant(ENST00000457726); non_coding_transcript_variant(ENST00000486102, ENST00000487805); upstream_gene_variant(ENST00000494005)
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)
RNF123	ring finger protein 123	3p24.3	Mapped by LD-proxy

SNPs in LD with rs6785549 (count: 0) View in gBrowse (chr3:49699132..49699132 )

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

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