Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (G)
Location

Chromosome 10:100216606 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.100216606G>A

Variation displays