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rs797044845

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044845(A;A)
Make rs797044845(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161307311
GeneMPZ
is asnp
is mentioned by
dbSNPrs797044845
ebirs797044845
HLIrs797044845
Exacrs797044845
Varsomers797044845
Maprs797044845
PheGenIrs797044845
hapmaprs797044845
1000 genomesrs797044845
hgdprs797044845
ensemblrs797044845
gopubmedrs797044845
geneviewrs797044845
scholarrs797044845
googlers797044845
pharmgkbrs797044845
gwascentralrs797044845
openSNPrs797044845
23andMers797044845
23andMe allrs797044845
SNP Nexus

SNPshotrs797044845
SNPdbers797044845
MSV3drs797044845
GWAS Ctlgrs797044845
Max Magnitude0
ClinVar
Risk rs797044845(A;A)
Alt rs797044845(A;A)
Reference rs797044845(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.161277101C>T
CLNSRC
CLNACC RCV000193325.1,