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rs863224449

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224449(C;G)
Make rs863224449(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161306737
GeneMPZ
is asnp
is mentioned by
dbSNPrs863224449
ebirs863224449
HLIrs863224449
Exacrs863224449
Varsomers863224449
Maprs863224449
PheGenIrs863224449
hapmaprs863224449
1000 genomesrs863224449
hgdprs863224449
ensemblrs863224449
gopubmedrs863224449
geneviewrs863224449
scholarrs863224449
googlers863224449
pharmgkbrs863224449
gwascentralrs863224449
openSNPrs863224449
23andMers863224449
23andMe allrs863224449
SNP Nexus

SNPshotrs863224449
SNPdbers863224449
MSV3drs863224449
GWAS Ctlgrs863224449
Max Magnitude0
ClinVar
Risk rs863224449(G;G)
Alt rs863224449(G;G)
Reference rs863224449(C;C)
Significance Probable-Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MPZ
CLNDBN Charcot-Marie-Tooth disease, type I
Reversed 1
HGVS NC_000001.10:g.161276527G>C
CLNSRC
CLNACC RCV000198501.1,