rs1057516798

Orientation

minus

Stabilized

minus

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

Make rs1057516798(C;C)

Make rs1057516798(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

36222887

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs1057516798
dbSNP (classic)	rs1057516798
ClinGen	rs1057516798
ebi	rs1057516798
HLI	rs1057516798
Exac	rs1057516798
Gnomad	rs1057516798
Varsome	rs1057516798
LitVar	rs1057516798
Map	rs1057516798
PheGenI	rs1057516798
Biobank	rs1057516798
1000 genomes	rs1057516798
hgdp	rs1057516798
ensembl	rs1057516798
geneview	rs1057516798
scholar	rs1057516798
google	rs1057516798
pharmgkb	rs1057516798
gwascentral	rs1057516798
openSNP	rs1057516798
23andMe	rs1057516798
SNPshot	rs1057516798
SNPdbe	rs1057516798
MSV3d	rs1057516798
GWAS Ctlg	rs1057516798

Max Magnitude

0

ClinVar
Risk	rs1057516798(C;C)
Alt	rs1057516798(C;C)
Reference	Rs1057516798(T;T)
Significance	Probable-Pathogenic
Disease	Inclusion body myopathy 2
Variation	info
Gene	GNE
CLNDBN	Inclusion body myopathy 2
Reversed	1
HGVS	NC_000009.11:g.36222884A>G
CLNSRC
CLNACC	RCV000411466.1,