Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 10:101769683 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.101769683T>A

Variation displays