Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.07 (C)
Location

Chromosome 6:3152285 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57111181, rs3799226

This variation has 13 HGVS names - click the plus to show

Variation displays