Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.15 (C)
Location

Chromosome 19:44908684 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749517 (T/C) ; HGMD-PUBLIC CM900020

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

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

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

Variation displays