Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 7:97025691 (forward strand) | View in location tab

Most severe consequence
HGVS name

7:g.97025691G>A

Variation displays