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rs724159959

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs724159959(G;G)
Make rs724159959(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position68929240
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs724159959
ebirs724159959
HLIrs724159959
Exacrs724159959
Varsomers724159959
Maprs724159959
PheGenIrs724159959
hapmaprs724159959
1000 genomesrs724159959
hgdprs724159959
ensemblrs724159959
gopubmedrs724159959
geneviewrs724159959
scholarrs724159959
googlers724159959
pharmgkbrs724159959
gwascentralrs724159959
openSNPrs724159959
23andMers724159959
23andMe allrs724159959
SNP Nexus

SNPshotrs724159959
SNPdbers724159959
MSV3drs724159959
GWAS Ctlgrs724159959
Max Magnitude0
ClinVar
Risk rs724159959(G;G)
Alt rs724159959(G;G)
Reference rs724159959(T;T)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene IGHMBP2
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2S
Reversed 0
HGVS NC_000011.9:g.68696708T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149577.4,