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rs387907036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907036(C;G)
Make rs387907036(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position104701677
GeneINF2
is asnp
is mentioned by
dbSNPrs387907036
ebirs387907036
HLIrs387907036
Exacrs387907036
Varsomers387907036
Maprs387907036
PheGenIrs387907036
hapmaprs387907036
1000 genomesrs387907036
hgdprs387907036
ensemblrs387907036
gopubmedrs387907036
geneviewrs387907036
scholarrs387907036
googlers387907036
pharmgkbrs387907036
gwascentralrs387907036
openSNPrs387907036
23andMers387907036
23andMe allrs387907036
SNP Nexus

SNPshotrs387907036
SNPdbers387907036
MSV3drs387907036
GWAS Ctlgrs387907036
Max Magnitude0
ClinVar
Risk rs387907036(G;G)
Alt rs387907036(G;G)
Reference rs387907036(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene INF2
CLNDBN Charcot-Marie-Tooth disease, dominant intermediate E
Reversed 0
HGVS NC_000014.8:g.105168014C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023851.2,