rs786204476

Orientation

minus

Stabilized

minus

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

Make rs786204476(A;A)

Make rs786204476(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

36246035

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs786204476
dbSNP (classic)	rs786204476
ClinGen	rs786204476
ebi	rs786204476
HLI	rs786204476
Exac	rs786204476
Gnomad	rs786204476
Varsome	rs786204476
LitVar	rs786204476
Map	rs786204476
PheGenI	rs786204476
Biobank	rs786204476
1000 genomes	rs786204476
hgdp	rs786204476
ensembl	rs786204476
geneview	rs786204476
scholar	rs786204476
google	rs786204476
pharmgkb	rs786204476
gwascentral	rs786204476
openSNP	rs786204476
23andMe	rs786204476
SNPshot	rs786204476
SNPdbe	rs786204476
MSV3d	rs786204476
GWAS Ctlg	rs786204476

Max Magnitude

0

ClinVar
Risk	rs786204476(A;A)
Alt	rs786204476(A;A)
Reference	Rs786204476(G;G)
Significance	Probable-Pathogenic
Disease	Inclusion body myopathy 2
Variation	info
Gene	GNE
CLNDBN	Inclusion body myopathy 2
Reversed	1
HGVS	NC_000009.11:g.36246032C>T
CLNSRC
CLNACC	RCV000169126.1,