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rs369061090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs369061090(A;A)
Make rs369061090(A;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position210606897
GeneCPS1
is asnp
is mentioned by
dbSNPrs369061090
dbSNP (classic)rs369061090
ClinGenrs369061090
ebirs369061090
HLIrs369061090
Exacrs369061090
Gnomadrs369061090
Varsomers369061090
LitVarrs369061090
Maprs369061090
PheGenIrs369061090
Biobankrs369061090
1000 genomesrs369061090
hgdprs369061090
ensemblrs369061090
geneviewrs369061090
scholarrs369061090
googlers369061090
pharmgkbrs369061090
gwascentralrs369061090
openSNPrs369061090
23andMers369061090
SNPshotrs369061090
SNPdbers369061090
MSV3drs369061090
GWAS Ctlgrs369061090
Max Magnitude0
ClinVar
Risk rs369061090(A;A)
Alt rs369061090(A;A)
Reference Rs369061090(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CPS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.211471621T>A
CLNSRC
CLNACC RCV000344019.1,