Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 3:46859495 (forward strand) | View in location tab

Co-located

with COSMIC COSM1423463 (C/T) ; HGMD-PUBLIC CM961008 ; PhenCode FHC0335 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Variation displays