Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 14:23425798 (forward strand) | View in location tab


with COSMIC COSM404544 (G/A) ; HGMD-PUBLIC CM011799

Most severe consequence
Evidence status

Clinical significance


LSDB 4217

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts and is associated with 3 phenotypes.

Variation displays