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rs797045102

From SNPedia

Orientationminus
Make rs797045102(-;-)
Make rs797045102(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position40396063
GenePRX
is asnp
is mentioned by
dbSNPrs797045102
ebirs797045102
HLIrs797045102
Exacrs797045102
Varsomers797045102
Maprs797045102
PheGenIrs797045102
hapmaprs797045102
1000 genomesrs797045102
hgdprs797045102
ensemblrs797045102
gopubmedrs797045102
geneviewrs797045102
scholarrs797045102
googlers797045102
pharmgkbrs797045102
gwascentralrs797045102
openSNPrs797045102
23andMers797045102
23andMe allrs797045102
SNP Nexus

SNPshotrs797045102
SNPdbers797045102
MSV3drs797045102
GWAS Ctlgrs797045102
Max Magnitude
ClinVar
Risk rs797045102(;)
Alt rs797045102(;)
Reference rs797045102(T;T)
Significance Probable-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.40901970delA
CLNSRC
CLNACC RCV000190618.1,