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rs587777712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777712(C;C)
Make rs587777712(C;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position1882687
GeneARHGEF10
is asnp
is mentioned by
dbSNPrs587777712
ebirs587777712
HLIrs587777712
Exacrs587777712
Varsomers587777712
Maprs587777712
PheGenIrs587777712
hapmaprs587777712
1000 genomesrs587777712
hgdprs587777712
ensemblrs587777712
gopubmedrs587777712
geneviewrs587777712
scholarrs587777712
googlers587777712
pharmgkbrs587777712
gwascentralrs587777712
openSNPrs587777712
23andMers587777712
23andMe allrs587777712
SNP Nexus

SNPshotrs587777712
SNPdbers587777712
MSV3drs587777712
GWAS Ctlgrs587777712
Max Magnitude0
ClinVar
Risk rs587777712(C;C)
Alt rs587777712(C;C)
Reference rs587777712(G;G)
Significance Probable-Pathogenic
Disease not provided Charcot-Marie-Tooth disease
Variation info
Gene ARHGEF10
CLNDBN not provided Charcot-Marie-Tooth disease
Reversed 0
HGVS NC_000008.10:g.1830853G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144070.3, RCV000144884.1,