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rs863225026

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(CCTCCCCCAGACGCC;CCTCCCCCAGACGCC) 0 common in clinvar
Make rs863225026(-;-)
Make rs863225026(-;CCTCCCCCAGACGCC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161305973
GeneMPZ
is asnp
is mentioned by
dbSNPrs863225026
dbSNP (old)rs863225026
ClinGenrs863225026
ebirs863225026
HLIrs863225026
Exacrs863225026
Gnomadrs863225026
Varsomers863225026
Maprs863225026
PheGenIrs863225026
Biobankrs863225026
1000 genomesrs863225026
hgdprs863225026
ensemblrs863225026
gopubmedrs863225026
geneviewrs863225026
scholarrs863225026
googlers863225026
pharmgkbrs863225026
gwascentralrs863225026
openSNPrs863225026
23andMers863225026
23andMe allrs863225026
SNP Nexus

SNPshotrs863225026
SNPdbers863225026
MSV3drs863225026
GWAS Ctlgrs863225026
Max Magnitude0
ClinVar
Risk rs863225026(-;-)
Alt rs863225026(-;-)
Reference Rs863225026(CCTCCCCCAGACGCC;CCTCCCCCAGACGCC)
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.161275763_161275777delGGCGTCTGGGGGAGG
CLNSRC Quest Diagnostics
CLNACC RCV000201070.1,