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rs797044870

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044870(A;G)
Make rs797044870(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position22086456
GeneCDC42
is asnp
is mentioned by
dbSNPrs797044870
ebirs797044870
HLIrs797044870
Exacrs797044870
Varsomers797044870
Maprs797044870
PheGenIrs797044870
hapmaprs797044870
1000 genomesrs797044870
hgdprs797044870
ensemblrs797044870
gopubmedrs797044870
geneviewrs797044870
scholarrs797044870
googlers797044870
pharmgkbrs797044870
gwascentralrs797044870
openSNPrs797044870
23andMers797044870
23andMe allrs797044870
SNP Nexus

SNPshotrs797044870
SNPdbers797044870
MSV3drs797044870
GWAS Ctlgrs797044870
Max Magnitude0
ClinVar
Risk rs797044870(G;G)
Alt rs797044870(G;G)
Reference rs797044870(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CDC42
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.22412949A>G
CLNSRC
CLNACC RCV000190678.1,