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rs762106720

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762106720(A;A)
Make rs762106720(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position36234073
GeneGNE
is asnp
is mentioned by
dbSNPrs762106720
ebirs762106720
HLIrs762106720
Exacrs762106720
Varsomers762106720
Maprs762106720
PheGenIrs762106720
hapmaprs762106720
1000 genomesrs762106720
hgdprs762106720
ensemblrs762106720
gopubmedrs762106720
geneviewrs762106720
scholarrs762106720
googlers762106720
pharmgkbrs762106720
gwascentralrs762106720
openSNPrs762106720
23andMers762106720
23andMe allrs762106720
SNP Nexus

SNPshotrs762106720
SNPdbers762106720
MSV3drs762106720
GWAS Ctlgrs762106720
Max Magnitude0
ClinVar
Risk rs762106720(A;A)
Alt rs762106720(A;A)
Reference rs762106720(G;G)
Significance Probable-Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36234070G>A
CLNSRC
CLNACC RCV000169197.1,