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rs387907341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907341(A;G)
Make rs387907341(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position179416495
GeneGNB4
is asnp
is mentioned by
dbSNPrs387907341
ebirs387907341
HLIrs387907341
Exacrs387907341
Varsomers387907341
Maprs387907341
PheGenIrs387907341
hapmaprs387907341
1000 genomesrs387907341
hgdprs387907341
ensemblrs387907341
gopubmedrs387907341
geneviewrs387907341
scholarrs387907341
googlers387907341
pharmgkbrs387907341
gwascentralrs387907341
openSNPrs387907341
23andMers387907341
23andMe allrs387907341
SNP Nexus

SNPshotrs387907341
SNPdbers387907341
MSV3drs387907341
GWAS Ctlgrs387907341
Max Magnitude0
ClinVar
Risk rs387907341(G;G)
Alt rs387907341(G;G)
Reference rs387907341(A;A)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene GNB4
CLNDBN Charcot-Marie-Tooth disease, dominant intermediate F
Reversed 1
HGVS NC_000003.11:g.179134283T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000034851.4,