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rs281865062

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865062(-;-)
Make rs281865062(-;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position40396254
GenePRX
is asnp
is mentioned by
dbSNPrs281865062
ebirs281865062
HLIrs281865062
Exacrs281865062
Varsomers281865062
Maprs281865062
PheGenIrs281865062
hapmaprs281865062
1000 genomesrs281865062
hgdprs281865062
ensemblrs281865062
gopubmedrs281865062
geneviewrs281865062
scholarrs281865062
googlers281865062
pharmgkbrs281865062
gwascentralrs281865062
openSNPrs281865062
23andMers281865062
23andMe allrs281865062
SNP Nexus

SNPshotrs281865062
SNPdbers281865062
MSV3drs281865062
GWAS Ctlgrs281865062
Max Magnitude0
ClinVar
Risk rs281865062(;)
Alt rs281865062(;)
Reference rs281865062(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene PRX
CLNDBN Charcot-Marie-Tooth disease, demyelinating, type 4f
Reversed 1
HGVS NC_000019.9:g.40902161delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000032003.1,