Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.30 (C)
Location

Chromosome 2:118078449 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR062118

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61203538

HGVS name

2:g.118078449C>G

This variation has assays on 6 chips - click the plus to show

Variation displays