Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/A/G | Ancestral: T | Ambiguity code: D
Location

Chromosome 6:32578852 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34274884, rs3816985

This variation has 6 HGVS names - click the plus to show

Variation displays