Original source

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

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

Chromosome 19:55545805 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74258005

HGVS name

19:g.55545805A>G

Variation displays