rs1057516657

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(GA;GA)	0	common in clinvar

Make rs1057516657(-;-)

Make rs1057516657(-;GA)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

36222866

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs1057516657
dbSNP (classic)	rs1057516657
ClinGen	rs1057516657
ebi	rs1057516657
HLI	rs1057516657
Exac	rs1057516657
Gnomad	rs1057516657
Varsome	rs1057516657
LitVar	rs1057516657
Map	rs1057516657
PheGenI	rs1057516657
Biobank	rs1057516657
1000 genomes	rs1057516657
hgdp	rs1057516657
ensembl	rs1057516657
geneview	rs1057516657
scholar	rs1057516657
google	rs1057516657
pharmgkb	rs1057516657
gwascentral	rs1057516657
openSNP	rs1057516657
23andMe	rs1057516657
SNPshot	rs1057516657
SNPdbe	rs1057516657
MSV3d	rs1057516657
GWAS Ctlg	rs1057516657

Max Magnitude

0

ClinVar
Risk	rs1057516657(-;-)
Alt	rs1057516657(-;-)
Reference	Rs1057516657(GA;GA)
Significance	Probable-Pathogenic
Disease	Inclusion body myopathy 2
Variation	info
Gene	GNE
CLNDBN	Inclusion body myopathy 2
Reversed	1
HGVS	NC_000009.11:g.36222863_36222864delTC
CLNSRC
CLNACC	RCV000411921.1,