Original source

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

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

Chromosome 5:135382095 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971473, CM991173

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 22912, 10443

This variation has 20 HGVS names - click the plus to show

Variation displays