Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)

Chromosome 19:1223126 (forward strand) | View in location tab


with COSMIC COSM21360 (C/G) ; HGMD-PUBLIC CM041082

Most severe consequence
Evidence status

Clinical significance


LSDB 10866

This variation has 9 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 1092 individual genotypes and is associated with 5 phenotypes.

Variation displays