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: 0.14 (G)
Location

Chromosome 11:89922329 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59154156, rs34355950

HGVS name

11:g.89922329G>A

Variation displays