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rs267606928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606928(C;T)
Make rs267606928(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position13125989
GeneOPTN
is asnp
is mentioned by
dbSNPrs267606928
ebirs267606928
HLIrs267606928
Exacrs267606928
Varsomers267606928
Maprs267606928
PheGenIrs267606928
hapmaprs267606928
1000 genomesrs267606928
hgdprs267606928
ensemblrs267606928
gopubmedrs267606928
geneviewrs267606928
scholarrs267606928
googlers267606928
pharmgkbrs267606928
gwascentralrs267606928
openSNPrs267606928
23andMers267606928
23andMe allrs267606928
SNP Nexus

SNPshotrs267606928
SNPdbers267606928
MSV3drs267606928
GWAS Ctlgrs267606928
Max Magnitude0
ClinVar
Risk rs267606928(G,T;G,T)
Alt rs267606928(G,T;G,T)
Reference rs267606928(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 12
Variation info
Gene OPTN
CLNDBN Amyotrophic lateral sclerosis type 12
Reversed 0
HGVS NC_000010.10:g.13167989C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007519.3,