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rs869312941

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312941(C;T)
Make rs869312941(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position63665930
GeneARHGEF9
is asnp
is mentioned by
dbSNPrs869312941
ebirs869312941
HLIrs869312941
Exacrs869312941
Varsomers869312941
Maprs869312941
PheGenIrs869312941
hapmaprs869312941
1000 genomesrs869312941
hgdprs869312941
ensemblrs869312941
gopubmedrs869312941
geneviewrs869312941
scholarrs869312941
googlers869312941
pharmgkbrs869312941
gwascentralrs869312941
openSNPrs869312941
23andMers869312941
23andMe allrs869312941
SNP Nexus

SNPshotrs869312941
SNPdbers869312941
MSV3drs869312941
GWAS Ctlgrs869312941
Max Magnitude0
ClinVar
Risk rs869312941(T;T)
Alt rs869312941(T;T)
Reference rs869312941(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ARHGEF9
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.62885810G>A
CLNSRC
CLNACC RCV000210722.1,