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 9:2645603 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080620

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003383.3:c.1342C>T, 27242

This variation has 8 HGVS names - click the plus to show

Variation displays