Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.30 (C)
Location

Chromosome 5:150843825 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56456031, rs57395593

HGVS name

5:g.150843825T>C

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3866 sample genotypes, is associated with 1 phenotype and is mentioned in 80 citations.

Variant displays