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rs387906790

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906790(A;A)
Make rs387906790(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35059723
GeneVCP
is asnp
is mentioned by
dbSNPrs387906790
ebirs387906790
HLIrs387906790
Exacrs387906790
Varsomers387906790
Maprs387906790
PheGenIrs387906790
hapmaprs387906790
1000 genomesrs387906790
hgdprs387906790
ensemblrs387906790
gopubmedrs387906790
geneviewrs387906790
scholarrs387906790
googlers387906790
pharmgkbrs387906790
gwascentralrs387906790
openSNPrs387906790
23andMers387906790
23andMe allrs387906790
SNP Nexus

SNPshotrs387906790
SNPdbers387906790
MSV3drs387906790
GWAS Ctlgrs387906790
Max Magnitude0
ClinVar
Risk rs387906790(A;A)
Alt rs387906790(A;A)
Reference rs387906790(G;G)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis 14 without frontotemporal dementia
Variation info
Gene VCP
CLNDBN Amyotrophic lateral sclerosis 14 without frontotemporal dementia
Reversed 1
HGVS NC_000009.11:g.35059720C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023066.2,