Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.22 (G)
Location

Chromosome 12:13563041 (forward strand) | View in location tab

Co-located

with COSMIC COSM3998717 (A/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.11:g.13715975A>G

This variation has 3 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 3807 individual genotypes, is associated with 2 phenotypes and is mentioned in 9 citations.

Variation displays