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rs864622732

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864622732(A;T)
Make rs864622732(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161307386
GeneMPZ
is asnp
is mentioned by
dbSNPrs864622732
ebirs864622732
HLIrs864622732
Exacrs864622732
Varsomers864622732
Maprs864622732
PheGenIrs864622732
hapmaprs864622732
1000 genomesrs864622732
hgdprs864622732
ensemblrs864622732
gopubmedrs864622732
geneviewrs864622732
scholarrs864622732
googlers864622732
pharmgkbrs864622732
gwascentralrs864622732
openSNPrs864622732
23andMers864622732
23andMe allrs864622732
SNP Nexus

SNPshotrs864622732
SNPdbers864622732
MSV3drs864622732
GWAS Ctlgrs864622732
Max Magnitude0
ClinVar
Risk rs864622732(T;T)
Alt rs864622732(T;T)
Reference rs864622732(A;A)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MPZ
CLNDBN Charcot-Marie-Tooth disease, type I
Reversed 1
HGVS NC_000001.10:g.161277176T>A
CLNSRC
CLNACC RCV000204639.1,