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 11:6394006 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM093884

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000543.4:c.1451C>T, 18034

This variation has 24 HGVS names - click the plus to show

Variation displays