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: 0.45 (G)
Location

Chromosome 19:55989684 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1264630, rs591690, rs60554045

HGVS name

19:g.55989684A>G

This variation has assays on 9 chips - click the plus to show

Variation displays