Original source

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

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

Chromosome 12:49658588 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs35706793, rs11168945

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

Variation displays