Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.13 (G)

Chromosome 12:49264805 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs35706793, rs11168945

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 1360 individual genotypes.

Variation displays