SNP Report

Basic Info

Name	rs4855862 dbSNP Ensembl
Location	chr3:49711400 - 49711400(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.415735
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000327697, ENST00000432042, ENST00000457726, ENST00000486102, ENST00000487805); NMD_transcript_variant(ENST00000457726); non_coding_transcript_variant(ENST00000486102, ENST00000487805); upstream_gene_variant(ENST00000433785, ENST00000444689, ENST00000469978)
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 rs4855862 (count: 0) View in gBrowse (chr3:49711400..49711400 )

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

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