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rs886041390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position31191431
GeneFUS
is asnp
is mentioned by
dbSNPrs886041390
dbSNP (classic)rs886041390
ClinGenrs886041390
ebirs886041390
HLIrs886041390
Exacrs886041390
Gnomadrs886041390
Varsomers886041390
LitVarrs886041390
Maprs886041390
PheGenIrs886041390
Biobankrs886041390
1000 genomesrs886041390
hgdprs886041390
ensemblrs886041390
geneviewrs886041390
scholarrs886041390
googlers886041390
pharmgkbrs886041390
gwascentralrs886041390
openSNPrs886041390
23andMers886041390
SNPshotrs886041390
SNPdbers886041390
MSV3drs886041390
GWAS Ctlgrs886041390
Max Magnitude0
ClinVar
Risk rs886041390(T;T)
Alt rs886041390(T;T)
Reference Rs886041390(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FUS
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.31202752C>T
CLNSRC
CLNACC RCV000381069.1,