Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 1:11796321 (forward strand) | View in location tab

Co-located

with COSMIC COSM146404 (G/A), COSM3927609 (G/A) ; HGMD-PUBLIC CM950819

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 4454 individual genotypes, is associated with 4 phenotypes and is mentioned in 426 citations.

Variation displays