Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 19:46729219 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58273978, rs17660257

HGVS name

19:g.46729219G>A

Variation displays