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rs62541771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62541771(A;A)
Make rs62541771(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position36218224
GeneGNE
is asnp
is mentioned by
dbSNPrs62541771
ebirs62541771
HLIrs62541771
Exacrs62541771
Varsomers62541771
Maprs62541771
PheGenIrs62541771
hapmaprs62541771
1000 genomesrs62541771
hgdprs62541771
ensemblrs62541771
gopubmedrs62541771
geneviewrs62541771
scholarrs62541771
googlers62541771
pharmgkbrs62541771
gwascentralrs62541771
openSNPrs62541771
23andMers62541771
23andMe allrs62541771
SNP Nexus

SNPshotrs62541771
SNPdbers62541771
MSV3drs62541771
GWAS Ctlgrs62541771
Max Magnitude0
OMIM603824
Desc
Variant0015
Relatedalso


ClinVar
Risk rs62541771(A;A)
Alt rs62541771(A;A)
Reference rs62541771(G;G)
Significance Pathogenic
Disease Nonaka myopathy Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Nonaka myopathy Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36218221G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006406.4, RCV000174039.1,