rs62541771

Orientation

plus

Stabilized

plus

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

Make rs62541771(A;A)

Make rs62541771(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

36218224

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs62541771
dbSNP (classic)	rs62541771
ClinGen	rs62541771
ebi	rs62541771
HLI	rs62541771
Exac	rs62541771
Gnomad	rs62541771
Varsome	rs62541771
LitVar	rs62541771
Map	rs62541771
PheGenI	rs62541771
Biobank	rs62541771
1000 genomes	rs62541771
hgdp	rs62541771
ensembl	rs62541771
geneview	rs62541771
scholar	rs62541771
google	rs62541771
pharmgkb	rs62541771
gwascentral	rs62541771
openSNP	rs62541771
23andMe	rs62541771
SNPshot	rs62541771
SNPdbe	rs62541771
MSV3d	rs62541771
GWAS Ctlg	rs62541771

Max Magnitude

0

OMIM	603824
Desc
Variant	0015
Related	also

ClinVar
Risk	rs62541771(A;A)
Alt	rs62541771(A;A)
Reference	Rs62541771(G;G)
Significance	Pathogenic
Disease	Nonaka myopathy Inclusion body myopathy 2 not provided Sialuria
Variation	info
Gene	GNE
CLNDBN	Nonaka myopathy Inclusion body myopathy 2 not provided Sialuria
Reversed	0
HGVS	NC_000009.11:g.36218221G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006406.6, RCV000174039.3, RCV000254883.1, RCV000265100.1,