Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs57395593, rs56456031

HGVS name

5:g.150843825T>C

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2634 individual genotypes, is associated with 1 phenotype and is mentioned in 79 citations.

Variation displays