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rs267607102

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607102(A;G)
Make rs267607102(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022196
GeneTARDBP
is asnp
is mentioned by
dbSNPrs267607102
ebirs267607102
HLIrs267607102
Exacrs267607102
Varsomers267607102
Maprs267607102
PheGenIrs267607102
hapmaprs267607102
1000 genomesrs267607102
hgdprs267607102
ensemblrs267607102
gopubmedrs267607102
geneviewrs267607102
scholarrs267607102
googlers267607102
pharmgkbrs267607102
gwascentralrs267607102
openSNPrs267607102
23andMers267607102
23andMe allrs267607102
SNP Nexus

SNPshotrs267607102
SNPdbers267607102
MSV3drs267607102
GWAS Ctlgrs267607102
Max Magnitude0
ClinVar
Risk rs267607102(G;G)
Alt rs267607102(G;G)
Reference rs267607102(A;A)
Significance Pathogenic
Disease FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS
Variation info
Gene TARDBP
CLNDBN FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
Reversed 0
HGVS NC_000001.10:g.11082253A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005549.2,