Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.18 (A)
Location

Chromosome 19:56057171 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74258005

HGVS name

19:g.56057171A>G

Variation displays