Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome 17:27756502 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.27756502A>G

Variation displays