Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 17:56594788 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990934

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_163_NOG_602991_0005, 11566

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

Variation displays