Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 17:56594888 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990937

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11569, 11562, 2010_April_001_160_NOG_602991_0001

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

Variation displays