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: 0.28 (G)
Location

Chromosome 12:52291312 (forward strand) | View in location tab

Co-located

with COSMIC COSM4147198 (C/G)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_018113

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays