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

rs387906789

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906789(C;G)
Make rs387906789(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35065352
GeneVCP
is asnp
is mentioned by
dbSNPrs387906789
ebirs387906789
HLIrs387906789
Exacrs387906789
Varsomers387906789
Maprs387906789
PheGenIrs387906789
hapmaprs387906789
1000 genomesrs387906789
hgdprs387906789
ensemblrs387906789
gopubmedrs387906789
geneviewrs387906789
scholarrs387906789
googlers387906789
pharmgkbrs387906789
gwascentralrs387906789
openSNPrs387906789
23andMers387906789
23andMe allrs387906789
SNP Nexus

SNPshotrs387906789
SNPdbers387906789
MSV3drs387906789
GWAS Ctlgrs387906789
Max Magnitude0
ClinVar
Risk rs387906789(G,T;G,T)
Alt rs387906789(G,T;G,T)
Reference rs387906789(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis 14
Variation info
Gene VCP
CLNDBN Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia
Reversed 1
HGVS NC_000009.11:g.35065349G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023065.3,