Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: T | Ambiguity code: S | MAF: 0.26 (C)
Location

Chromosome 13:28067433 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57898425

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2777 individual genotypes.

Variation displays