Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.39 (T)
Location

Chromosome 4:54100752 (forward strand) | View in location tab

Co-located

with COSMIC COSM1328491 (T/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2278140, rs3194385

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays