Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.22 (G)
Location

Chromosome 19:55547371 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58560270

HGVS name

19:g.55547371A>G

This variation has assays on 10 chips - click the plus to show

Variation displays