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rs1057518022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518022(A;A)
Make rs1057518022(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position22081740
GeneCDC42
is asnp
is mentioned by
dbSNPrs1057518022
dbSNP (old)rs1057518022
ClinGenrs1057518022
ebirs1057518022
HLIrs1057518022
Exacrs1057518022
Gnomadrs1057518022
Varsomers1057518022
Maprs1057518022
PheGenIrs1057518022
Biobankrs1057518022
1000 genomesrs1057518022
hgdprs1057518022
ensemblrs1057518022
gopubmedrs1057518022
geneviewrs1057518022
scholarrs1057518022
googlers1057518022
pharmgkbrs1057518022
gwascentralrs1057518022
openSNPrs1057518022
23andMers1057518022
23andMe allrs1057518022
SNPshotrs1057518022
SNPdbers1057518022
MSV3drs1057518022
GWAS Ctlgrs1057518022
Max Magnitude0
ClinVar
Risk rs1057518022(A;A)
Alt rs1057518022(A;A)
Reference Rs1057518022(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDC42
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.22408233G>A
CLNSRC
CLNACC RCV000414468.1,