rs1057516374

Orientation

minus

Stabilized

minus

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

Make rs1057516374(C;T)

Make rs1057516374(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

36233986

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs1057516374
dbSNP (classic)	rs1057516374
ClinGen	rs1057516374
ebi	rs1057516374
HLI	rs1057516374
Exac	rs1057516374
Gnomad	rs1057516374
Varsome	rs1057516374
LitVar	rs1057516374
Map	rs1057516374
PheGenI	rs1057516374
Biobank	rs1057516374
1000 genomes	rs1057516374
hgdp	rs1057516374
ensembl	rs1057516374
geneview	rs1057516374
scholar	rs1057516374
google	rs1057516374
pharmgkb	rs1057516374
gwascentral	rs1057516374
openSNP	rs1057516374
23andMe	rs1057516374
SNPshot	rs1057516374
SNPdbe	rs1057516374
MSV3d	rs1057516374
GWAS Ctlg	rs1057516374

Max Magnitude

0

ClinVar
Risk	rs1057516374(T;T)
Alt	rs1057516374(T;T)
Reference	Rs1057516374(C;C)
Significance	Probable-Pathogenic
Disease	Inclusion body myopathy 2
Variation	info
Gene	GNE
CLNDBN	Inclusion body myopathy 2
Reversed	1
HGVS	NC_000009.11:g.36233983G>A
CLNSRC
CLNACC	RCV000409849.1,