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rs786204476

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204476(A;A)
Make rs786204476(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position36246035
GeneGNE
is asnp
is mentioned by
dbSNPrs786204476
ebirs786204476
HLIrs786204476
Exacrs786204476
Varsomers786204476
Maprs786204476
PheGenIrs786204476
hapmaprs786204476
1000 genomesrs786204476
hgdprs786204476
ensemblrs786204476
gopubmedrs786204476
geneviewrs786204476
scholarrs786204476
googlers786204476
pharmgkbrs786204476
gwascentralrs786204476
openSNPrs786204476
23andMers786204476
23andMe allrs786204476
SNP Nexus

SNPshotrs786204476
SNPdbers786204476
MSV3drs786204476
GWAS Ctlgrs786204476
Max Magnitude0
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,