Original source

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

Alleles
G/A|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 12:52287296 (forward strand)|View in location tab

Co-located variant

PhenCode HIFD_KRT81:c.1053T>C (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs11170085, rs11552018

HGVS names

This variant has 7 HGVS names - Show

About this variant

Variant displays