Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 9:121310819 (forward strand) | View in location tab


with COSMIC COSM1459755 (G/A), COSM1459756 (G/A) ; HGMD-PUBLIC CM920315, CM910196

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 56 HGVS names - click the plus to show

About this variant

This variant overlaps 34 transcripts and is associated with 5 phenotypes.

Variation displays