Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 9:101866027 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.101866027A>T

Variation displays