Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:124073097 (forward strand) | View in location tab


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

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

Variation displays