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rs281865061

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865061(-;-)
Make rs281865061(-;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position40398754
GenePRX
is asnp
is mentioned by
dbSNPrs281865061
ebirs281865061
HLIrs281865061
Exacrs281865061
Varsomers281865061
Maprs281865061
PheGenIrs281865061
hapmaprs281865061
1000 genomesrs281865061
hgdprs281865061
ensemblrs281865061
gopubmedrs281865061
geneviewrs281865061
scholarrs281865061
googlers281865061
pharmgkbrs281865061
gwascentralrs281865061
openSNPrs281865061
23andMers281865061
23andMe allrs281865061
SNP Nexus

SNPshotrs281865061
SNPdbers281865061
MSV3drs281865061
GWAS Ctlgrs281865061
Max Magnitude0
ClinVar
Risk rs281865061(;)
Alt rs281865061(;)
Reference rs281865061(C;C)
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.40904661delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000032005.1,