Original source

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

Alleles
G/A | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 14:21633673 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.21633673G>A

Variation displays