Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 19:41970405 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042308

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5381, SCV000053410, NM_152296.3:c.2401G>T

This variation has 22 HGVS names - click the plus to show

Variation displays