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 18:51065521 (forward strand) | View in location tab


with COSMIC COSM1150607 (G/A) ; HGMD-PUBLIC CM024126

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, is associated with 6 phenotypes and is mentioned in 2 citations.

Variation displays