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rs267606929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606929(A;G)
Make rs267606929(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position13132098
GeneOPTN
is asnp
is mentioned by
dbSNPrs267606929
ebirs267606929
HLIrs267606929
Exacrs267606929
Varsomers267606929
Maprs267606929
PheGenIrs267606929
hapmaprs267606929
1000 genomesrs267606929
hgdprs267606929
ensemblrs267606929
gopubmedrs267606929
geneviewrs267606929
scholarrs267606929
googlers267606929
pharmgkbrs267606929
gwascentralrs267606929
openSNPrs267606929
23andMers267606929
23andMe allrs267606929
SNP Nexus

SNPshotrs267606929
SNPdbers267606929
MSV3drs267606929
GWAS Ctlgrs267606929
Max Magnitude0
ClinVar
Risk rs267606929(G;G)
Alt rs267606929(G;G)
Reference rs267606929(A;A)
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.13174098A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007520.3,