Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 19:48897512 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.48897512A>G

Variation displays