Have questions? Visit https://www.reddit.com/r/SNPedia

rs724159958

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs724159958(G;G)
Make rs724159958(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position68911496
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs724159958
ebirs724159958
HLIrs724159958
Exacrs724159958
Varsomers724159958
Maprs724159958
PheGenIrs724159958
hapmaprs724159958
1000 genomesrs724159958
hgdprs724159958
ensemblrs724159958
gopubmedrs724159958
geneviewrs724159958
scholarrs724159958
googlers724159958
pharmgkbrs724159958
gwascentralrs724159958
openSNPrs724159958
23andMers724159958
23andMe allrs724159958
SNP Nexus

SNPshotrs724159958
SNPdbers724159958
MSV3drs724159958
GWAS Ctlgrs724159958
Max Magnitude0
ClinVar
Risk rs724159958(G;G)
Alt rs724159958(G;G)
Reference rs724159958(T;T)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease
Variation info
Gene IGHMBP2
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2S Charcot-Marie-Tooth disease
Reversed 0
HGVS NC_000011.9:g.68678964T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149576.4, RCV000192259.1,