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rs863225025

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225025(A;A)
Make rs863225025(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161306746
GeneMPZ
is asnp
is mentioned by
dbSNPrs863225025
ebirs863225025
HLIrs863225025
Exacrs863225025
Varsomers863225025
Maprs863225025
PheGenIrs863225025
hapmaprs863225025
1000 genomesrs863225025
hgdprs863225025
ensemblrs863225025
gopubmedrs863225025
geneviewrs863225025
scholarrs863225025
googlers863225025
pharmgkbrs863225025
gwascentralrs863225025
openSNPrs863225025
23andMers863225025
23andMe allrs863225025
SNP Nexus

SNPshotrs863225025
SNPdbers863225025
MSV3drs863225025
GWAS Ctlgrs863225025
Max Magnitude0
ClinVar
Risk rs863225025(A;A)
Alt rs863225025(A;A)
Reference rs863225025(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MPZ
CLNDBN Charcot-Marie-Tooth disease, demyelinating, type 1b
Reversed 1
HGVS NC_000001.10:g.161276536C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201196.1,