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rs138226428

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138226428(C;T)
Make rs138226428(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position127487695
GeneLRSAM1
is asnp
is mentioned by
dbSNPrs138226428
ebirs138226428
HLIrs138226428
Exacrs138226428
Varsomers138226428
Maprs138226428
PheGenIrs138226428
hapmaprs138226428
1000 genomesrs138226428
hgdprs138226428
ensemblrs138226428
gopubmedrs138226428
geneviewrs138226428
scholarrs138226428
googlers138226428
pharmgkbrs138226428
gwascentralrs138226428
openSNPrs138226428
23andMers138226428
23andMe allrs138226428
SNP Nexus

SNPshotrs138226428
SNPdbers138226428
MSV3drs138226428
GWAS Ctlgrs138226428
Max Magnitude0
ClinVar
Risk rs138226428(T;T)
Alt rs138226428(T;T)
Reference rs138226428(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease type 2P
Variation info
Gene LRSAM1
CLNDBN Charcot-Marie-Tooth disease type 2P
Reversed 0
HGVS NC_000009.11:g.130249974C>T
CLNSRC
CLNACC RCV000231111.1,