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 22:51007141 (forward strand) | View in location tab

Most severe consequence
HGVS name

22:g.51007141G>T

Variation displays