Original source

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

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10866

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

This variation has assays on 4 chips - click the plus to show

Variation displays