Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 2:27136426 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.27136426G>C

Variation displays