Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.20 (C)
Location

Chromosome 4:38797027 (forward strand) | View in location tab

Co-located

with COSMIC COSM3760608 (C/A) ; HGMD-PUBLIC CM073378

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant overlaps 10 transcripts, has 2557 individual genotypes, is associated with 2 phenotypes and is mentioned in 32 citations.

Variation displays