Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606832(C;T)
Make rs267606832(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31185061
GeneFUS
is asnp
is mentioned by
dbSNPrs267606832
ClinGenrs267606832
ebirs267606832
HLIrs267606832
Exacrs267606832
Varsomers267606832
Maprs267606832
PheGenIrs267606832
hapmaprs267606832
1000 genomesrs267606832
hgdprs267606832
ensemblrs267606832
gopubmedrs267606832
geneviewrs267606832
scholarrs267606832
googlers267606832
pharmgkbrs267606832
gwascentralrs267606832
openSNPrs267606832
23andMers267606832
23andMe allrs267606832
SNP Nexus

SNPshotrs267606832
SNPdbers267606832
MSV3drs267606832
GWAS Ctlgrs267606832
Max Magnitude0
ClinVar
Risk rs267606832(T;T)
Alt rs267606832(T;T)
Reference Rs267606832(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 6 Tremor
Variation info
Gene FUS
CLNDBN Amyotrophic lateral sclerosis type 6 Tremor, hereditary essential, 4
Reversed 0
HGVS NC_000016.9:g.31196382C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017614.28, RCV000030719.24,