Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 17:56594838 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056014

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11577, 2010_April_001_171_NOG_602991_0016

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

Variation displays