Have questions? Visit https://www.reddit.com/r/SNPedia

rs387907340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907340(A;A)
Make rs387907340(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position179419444
GeneGNB4
is asnp
is mentioned by
dbSNPrs387907340
ebirs387907340
HLIrs387907340
Exacrs387907340
Varsomers387907340
Maprs387907340
PheGenIrs387907340
hapmaprs387907340
1000 genomesrs387907340
hgdprs387907340
ensemblrs387907340
gopubmedrs387907340
geneviewrs387907340
scholarrs387907340
googlers387907340
pharmgkbrs387907340
gwascentralrs387907340
openSNPrs387907340
23andMers387907340
23andMe allrs387907340
SNP Nexus

SNPshotrs387907340
SNPdbers387907340
MSV3drs387907340
GWAS Ctlgrs387907340
Max Magnitude0
ClinVar
Risk rs387907340(A;A)
Alt rs387907340(A;A)
Reference rs387907340(G;G)
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.179137232C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034850.4,