rs1057516364

Orientation

minus

Stabilized

minus

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

Make rs1057516364(C;C)

Make rs1057516364(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

36227267

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs1057516364
dbSNP (classic)	rs1057516364
ClinGen	rs1057516364
ebi	rs1057516364
HLI	rs1057516364
Exac	rs1057516364
Gnomad	rs1057516364
Varsome	rs1057516364
LitVar	rs1057516364
Map	rs1057516364
PheGenI	rs1057516364
Biobank	rs1057516364
1000 genomes	rs1057516364
hgdp	rs1057516364
ensembl	rs1057516364
geneview	rs1057516364
scholar	rs1057516364
google	rs1057516364
pharmgkb	rs1057516364
gwascentral	rs1057516364
openSNP	rs1057516364
23andMe	rs1057516364
SNPshot	rs1057516364
SNPdbe	rs1057516364
MSV3d	rs1057516364
GWAS Ctlg	rs1057516364

Max Magnitude

0

ClinVar
Risk	rs1057516364(C;C)
Alt	rs1057516364(C;C)
Reference	Rs1057516364(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.36227264A>G
CLNSRC
CLNACC	RCV000410389.1,