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rs387906628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906628(A;A)
Make rs387906628(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31185031
GeneFUS
is asnp
is mentioned by
dbSNPrs387906628
ebirs387906628
HLIrs387906628
Exacrs387906628
Varsomers387906628
Maprs387906628
PheGenIrs387906628
hapmaprs387906628
1000 genomesrs387906628
hgdprs387906628
ensemblrs387906628
gopubmedrs387906628
geneviewrs387906628
scholarrs387906628
googlers387906628
pharmgkbrs387906628
gwascentralrs387906628
openSNPrs387906628
23andMers387906628
23andMe allrs387906628
SNP Nexus

SNPshotrs387906628
SNPdbers387906628
MSV3drs387906628
GWAS Ctlgrs387906628
Max Magnitude0
ClinVar
Risk rs387906628(A;A)
Alt rs387906628(A;A)
Reference rs387906628(G;G)
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.31196352G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022557.29,