Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (G)

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


with COSMIC COSM3998717 (A/G)

Most severe consequence
Evidence status

Clinical significance


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 2400 individual genotypes, is associated with 2 phenotypes and is mentioned in 8 citations.

Variation displays