Original source

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

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

Chromosome 11:2150326 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.2150326G>A

Variation displays