Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)
Location

Chromosome 7:128829863 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs73721646

HGVS name

7:g.128829863T>C

Variation displays