Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 17:54671912 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022050

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11574, 2010_April_001_170_NOG_602991_0013

This variation has 3 HGVS names - click the plus to show

Variation displays