Original source

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

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

Chromosome 11:1994893 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.1994893G>A

Variation displays