Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 17:56594891 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990938

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_162_NOG_602991_0004, 11565

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

Variation displays