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rs895824243

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position13110387
GeneOPTN
is asnp
is mentioned by
dbSNPrs895824243
dbSNP (classic)rs895824243
ClinGenrs895824243
ebirs895824243
HLIrs895824243
Exacrs895824243
Gnomadrs895824243
Varsomers895824243
LitVarrs895824243
Maprs895824243
PheGenIrs895824243
Biobankrs895824243
1000 genomesrs895824243
hgdprs895824243
ensemblrs895824243
geneviewrs895824243
scholarrs895824243
googlers895824243
pharmgkbrs895824243
gwascentralrs895824243
openSNPrs895824243
23andMers895824243
23andMe allrs895824243
SNPshotrs895824243
SNPdbers895824243
MSV3drs895824243
GWAS Ctlgrs895824243
Max Magnitude0
ClinVar
Risk rs895824243(C;C)
Alt rs895824243(C;C)
Reference Rs895824243(A;A)
Significance Probable-Pathogenic
Disease Motor neuron disease
Variation info
Gene
CLNDBN Motor neuron disease
Reversed 0
HGVS NC_000010.10:g.13152387A>C
CLNSRC
CLNACC RCV000492199.1,