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 6:6151813 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS920751

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1817

This variation has 6 HGVS names - click the plus to show

Variation displays