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rs864309501

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309501(A;A)
Make rs864309501(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position35065274
GeneVCP
is asnp
is mentioned by
dbSNPrs864309501
ebirs864309501
HLIrs864309501
Exacrs864309501
Varsomers864309501
Maprs864309501
PheGenIrs864309501
hapmaprs864309501
1000 genomesrs864309501
hgdprs864309501
ensemblrs864309501
gopubmedrs864309501
geneviewrs864309501
scholarrs864309501
googlers864309501
pharmgkbrs864309501
gwascentralrs864309501
openSNPrs864309501
23andMers864309501
23andMe allrs864309501
SNP Nexus

SNPshotrs864309501
SNPdbers864309501
MSV3drs864309501
GWAS Ctlgrs864309501
Max Magnitude0
ClinVar
Risk rs864309501(A;A)
Alt rs864309501(A;A)
Reference rs864309501(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene VCP
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2y
Reversed 1
HGVS NC_000009.11:g.35065271C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202444.1,