Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.03 (G)
Location

Chromosome 2:208121117 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.208121117C>G

Variation displays