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rs387907274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907274(C;T)
Make rs387907274(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31189158
GeneFUS
is asnp
is mentioned by
dbSNPrs387907274
ebirs387907274
HLIrs387907274
Exacrs387907274
Varsomers387907274
Maprs387907274
PheGenIrs387907274
hapmaprs387907274
1000 genomesrs387907274
hgdprs387907274
ensemblrs387907274
gopubmedrs387907274
geneviewrs387907274
scholarrs387907274
googlers387907274
pharmgkbrs387907274
gwascentralrs387907274
openSNPrs387907274
23andMers387907274
23andMe allrs387907274
SNP Nexus

SNPshotrs387907274
SNPdbers387907274
MSV3drs387907274
GWAS Ctlgrs387907274
Max Magnitude0
ClinVar
Risk rs387907274(T;T)
Alt rs387907274(T;T)
Reference rs387907274(C;C)
Significance Pathogenic
Disease Tremor
Variation info
Gene FUS
CLNDBN Tremor, hereditary essential, 4
Reversed 0
HGVS NC_000016.9:g.31200479C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030720.27,