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 1:158685290 (forward strand) | View in location tab


with COSMIC COSM1335249 (G/A) ; HGMD-PUBLIC CM910359, CM910358

Most severe consequence
Clinical significance

This variation has 4 synonyms - click the plus to show

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

About this variant

This variant overlaps 7 transcripts and is associated with 6 phenotypes.

Variation displays