Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 17:56594609 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013954

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11571, 2010_April_001_168_NOG_602991_0010

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

Variation displays