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rs797044916

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044916(A;G)
Make rs797044916(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position22078546
GeneCDC42
is asnp
is mentioned by
dbSNPrs797044916
ebirs797044916
HLIrs797044916
Exacrs797044916
Varsomers797044916
Maprs797044916
PheGenIrs797044916
hapmaprs797044916
1000 genomesrs797044916
hgdprs797044916
ensemblrs797044916
gopubmedrs797044916
geneviewrs797044916
scholarrs797044916
googlers797044916
pharmgkbrs797044916
gwascentralrs797044916
openSNPrs797044916
23andMers797044916
23andMe allrs797044916
SNP Nexus

SNPshotrs797044916
SNPdbers797044916
MSV3drs797044916
GWAS Ctlgrs797044916
Max Magnitude0
ClinVar
Risk rs797044916(G;G)
Alt rs797044916(G;G)
Reference rs797044916(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CDC42
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.22405039A>G
CLNSRC
CLNACC RCV000190749.1,