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rs387907034

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907034(C;C)
Make rs387907034(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position104701675
GeneINF2
is asnp
is mentioned by
dbSNPrs387907034
ebirs387907034
HLIrs387907034
Exacrs387907034
Varsomers387907034
Maprs387907034
PheGenIrs387907034
hapmaprs387907034
1000 genomesrs387907034
hgdprs387907034
ensemblrs387907034
gopubmedrs387907034
geneviewrs387907034
scholarrs387907034
googlers387907034
pharmgkbrs387907034
gwascentralrs387907034
openSNPrs387907034
23andMers387907034
23andMe allrs387907034
SNP Nexus

SNPshotrs387907034
SNPdbers387907034
MSV3drs387907034
GWAS Ctlgrs387907034
Max Magnitude0
ClinVar
Risk rs387907034(C;C)
Alt rs387907034(C;C)
Reference rs387907034(T;T)
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.105168012T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023849.2,