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rs797044802

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044802(G;T)
Make rs797044802(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68908338
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs797044802
ebirs797044802
HLIrs797044802
Exacrs797044802
Varsomers797044802
Maprs797044802
PheGenIrs797044802
hapmaprs797044802
1000 genomesrs797044802
hgdprs797044802
ensemblrs797044802
gopubmedrs797044802
geneviewrs797044802
scholarrs797044802
googlers797044802
pharmgkbrs797044802
gwascentralrs797044802
openSNPrs797044802
23andMers797044802
23andMe allrs797044802
SNP Nexus

SNPshotrs797044802
SNPdbers797044802
MSV3drs797044802
GWAS Ctlgrs797044802
Max Magnitude0
ClinVar
Risk rs797044802(T;T)
Alt rs797044802(T;T)
Reference rs797044802(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene IGHMBP2
CLNDBN Charcot-Marie-Tooth disease
Reversed 0
HGVS NC_000011.9:g.68675806G>T
CLNSRC
CLNACC RCV000192263.1,