rs121908629

Orientation

minus

Stabilized

minus

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

Make rs121908629(A;A)

Make rs121908629(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

36236864

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs121908629
dbSNP (classic)	rs121908629
ClinGen	rs121908629
ebi	rs121908629
HLI	rs121908629
Exac	rs121908629
Gnomad	rs121908629
Varsome	rs121908629
LitVar	rs121908629
Map	rs121908629
PheGenI	rs121908629
Biobank	rs121908629
1000 genomes	rs121908629
hgdp	rs121908629
ensembl	rs121908629
geneview	rs121908629
scholar	rs121908629
google	rs121908629
pharmgkb	rs121908629
gwascentral	rs121908629
openSNP	rs121908629
23andMe	rs121908629
SNPshot	rs121908629
SNPdbe	rs121908629
MSV3d	rs121908629
GWAS Ctlg	rs121908629

Max Magnitude

0

OMIM	603824
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121908629(A;A) rs121908629(C;C)
Alt	rs121908629(A;A) rs121908629(C;C)
Reference	Rs121908629(G;G)
Significance	Other
Disease	Inclusion body myopathy 2 Nonaka myopathy
Variation	info
Gene	GNE
CLNDBN	Inclusion body myopathy 2 Nonaka myopathy
Reversed	1
HGVS	NC_000009.11:g.36236861C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006401.5, RCV000202425.1,