Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 19:41970533 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042306

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5379, NM_152296.3:c.2273T>G

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

Variation displays