Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.09 (C)
Location

Chromosome 6:3152051 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57111181, rs3799226

This variant has 12 HGVS names - click the plus to show

About this variant

Variant displays