Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.09 (C)
Location

Chromosome 6:32546711 (forward strand) | View in location tab

Co-located

with dbSNP rs1060173 (A/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34395043

This variation has 2 HGVS names - click the plus to show

Variation displays