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rs756985703

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756985703(A;A)
Make rs756985703(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68934517
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs756985703
ebirs756985703
HLIrs756985703
Exacrs756985703
Varsomers756985703
Maprs756985703
PheGenIrs756985703
hapmaprs756985703
1000 genomesrs756985703
hgdprs756985703
ensemblrs756985703
gopubmedrs756985703
geneviewrs756985703
scholarrs756985703
googlers756985703
pharmgkbrs756985703
gwascentralrs756985703
openSNPrs756985703
23andMers756985703
23andMe allrs756985703
SNP Nexus

SNPshotrs756985703
SNPdbers756985703
MSV3drs756985703
GWAS Ctlgrs756985703
Max Magnitude0
ClinVar
Risk rs756985703(A;A)
Alt rs756985703(A;A)
Reference rs756985703(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene IGHMBP2
CLNDBN Charcot-Marie-Tooth disease
Reversed 0
HGVS NC_000011.9:g.68701985C>A
CLNSRC
CLNACC RCV000192261.1,