Original source

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

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

Chromosome 11:116788979 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.116788979A>G

Variation displays