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rs267606833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606833(A;T)
Make rs267606833(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191427
GeneFUS
is asnp
is mentioned by
dbSNPrs267606833
ebirs267606833
HLIrs267606833
Exacrs267606833
Varsomers267606833
Maprs267606833
PheGenIrs267606833
hapmaprs267606833
1000 genomesrs267606833
hgdprs267606833
ensemblrs267606833
gopubmedrs267606833
geneviewrs267606833
scholarrs267606833
googlers267606833
pharmgkbrs267606833
gwascentralrs267606833
openSNPrs267606833
23andMers267606833
23andMe allrs267606833
SNP Nexus

SNPshotrs267606833
SNPdbers267606833
MSV3drs267606833
GWAS Ctlgrs267606833
Max Magnitude0
ClinVar
Risk rs267606833(T;T)
Alt rs267606833(T;T)
Reference rs267606833(A;A)
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.31202748A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017615.27,