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

rs864309502

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309502(A;A)
Make rs864309502(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position35067903
GeneVCP
is asnp
is mentioned by
dbSNPrs864309502
ebirs864309502
HLIrs864309502
Exacrs864309502
Varsomers864309502
Maprs864309502
PheGenIrs864309502
hapmaprs864309502
1000 genomesrs864309502
hgdprs864309502
ensemblrs864309502
gopubmedrs864309502
geneviewrs864309502
scholarrs864309502
googlers864309502
pharmgkbrs864309502
gwascentralrs864309502
openSNPrs864309502
23andMers864309502
23andMe allrs864309502
SNP Nexus

SNPshotrs864309502
SNPdbers864309502
MSV3drs864309502
GWAS Ctlgrs864309502
Max Magnitude0
ClinVar
Risk rs864309502(A;A)
Alt rs864309502(A;A)
Reference rs864309502(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.35067900C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202492.1,