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rs387906627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906627(C;T)
Make rs387906627(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191052
GeneFUS
is asnp
is mentioned by
dbSNPrs387906627
ebirs387906627
HLIrs387906627
Exacrs387906627
Varsomers387906627
Maprs387906627
PheGenIrs387906627
hapmaprs387906627
1000 genomesrs387906627
hgdprs387906627
ensemblrs387906627
gopubmedrs387906627
geneviewrs387906627
scholarrs387906627
googlers387906627
pharmgkbrs387906627
gwascentralrs387906627
openSNPrs387906627
23andMers387906627
23andMe allrs387906627
SNP Nexus

SNPshotrs387906627
SNPdbers387906627
MSV3drs387906627
GWAS Ctlgrs387906627
Max Magnitude0
ClinVar
Risk rs387906627(T;T)
Alt rs387906627(T;T)
Reference rs387906627(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 6
Variation info
Gene FUS
CLNDBN Amyotrophic lateral sclerosis type 6
Reversed 0
HGVS NC_000016.9:g.31202373C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022556.29,