Original source

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

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

Chromosome 3:87255907 (forward strand) | View in location tab

Most severe consequence
HGVS name

3:g.87255907T>G

Variation displays