Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 19:41978041 (forward strand) | View in location tab

Co-located

with COSMIC COSM3389055 (G/A) ; HGMD-PUBLIC CM042305

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_152296.3:c.1838C>T, 5376

This variation has 11 HGVS names - click the plus to show

Variation displays