Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 1:27340382 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.27340382G>T

Variation displays