rs1057516965

Orientation

minus

Stabilized

minus

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

Make rs1057516965(-;-)

Make rs1057516965(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

36222993

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs1057516965
dbSNP (classic)	rs1057516965
ClinGen	rs1057516965
ebi	rs1057516965
HLI	rs1057516965
Exac	rs1057516965
Gnomad	rs1057516965
Varsome	rs1057516965
LitVar	rs1057516965
Map	rs1057516965
PheGenI	rs1057516965
Biobank	rs1057516965
1000 genomes	rs1057516965
hgdp	rs1057516965
ensembl	rs1057516965
geneview	rs1057516965
scholar	rs1057516965
google	rs1057516965
pharmgkb	rs1057516965
gwascentral	rs1057516965
openSNP	rs1057516965
23andMe	rs1057516965
SNPshot	rs1057516965
SNPdbe	rs1057516965
MSV3d	rs1057516965
GWAS Ctlg	rs1057516965

Max Magnitude

0

ClinVar
Risk	rs1057516965(-;-)
Alt	rs1057516965(-;-)
Reference	Rs1057516965(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.36222990delA
CLNSRC
CLNACC	RCV000411761.1,