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rs202191898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202191898(C;T)
Make rs202191898(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position6468378
GenePLEKHG5
is asnp
is mentioned by
dbSNPrs202191898
ebirs202191898
HLIrs202191898
Exacrs202191898
Varsomers202191898
Maprs202191898
PheGenIrs202191898
hapmaprs202191898
1000 genomesrs202191898
hgdprs202191898
ensemblrs202191898
gopubmedrs202191898
geneviewrs202191898
scholarrs202191898
googlers202191898
pharmgkbrs202191898
gwascentralrs202191898
openSNPrs202191898
23andMers202191898
23andMe allrs202191898
SNP Nexus

SNPshotrs202191898
SNPdbers202191898
MSV3drs202191898
GWAS Ctlgrs202191898
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs202191898(G,T;G,T)
Alt rs202191898(G,T;G,T)
Reference rs202191898(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease not specified
Variation info
Gene TNFRSF25 PLEKHG5
CLNDBN Charcot-Marie-Tooth disease, recessive intermediate c not specified
Reversed 0
HGVS NC_000001.10:g.6528438C>G; NC_000001.10:g.6528438C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054546.4, RCV000221669.1,