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rs121908395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908395(C;C)
Make rs121908395(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022278
GeneTARDBP
is asnp
is mentioned by
dbSNPrs121908395
ebirs121908395
HLIrs121908395
Exacrs121908395
Varsomers121908395
Maprs121908395
PheGenIrs121908395
hapmaprs121908395
1000 genomesrs121908395
hgdprs121908395
ensemblrs121908395
gopubmedrs121908395
geneviewrs121908395
scholarrs121908395
googlers121908395
pharmgkbrs121908395
gwascentralrs121908395
openSNPrs121908395
23andMers121908395
23andMe allrs121908395
SNP Nexus

SNPshotrs121908395
SNPdbers121908395
MSV3drs121908395
GWAS Ctlgrs121908395
Max Magnitude0
OMIM605078
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908395(C;C)
Alt rs121908395(C;C)
Reference rs121908395(G;G)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 10
Variation info
Gene TARDBP
CLNDBN Amyotrophic lateral sclerosis type 10
Reversed 0
HGVS NC_000001.10:g.11082335G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005542.3,