Have questions? Visit https://www.reddit.com/r/SNPedia

rs758724746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758724746(A;A)
Make rs758724746(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position210608507
GeneCPS1
is asnp
is mentioned by
dbSNPrs758724746
dbSNP (classic)rs758724746
ClinGenrs758724746
ebirs758724746
HLIrs758724746
Exacrs758724746
Gnomadrs758724746
Varsomers758724746
LitVarrs758724746
Maprs758724746
PheGenIrs758724746
Biobankrs758724746
1000 genomesrs758724746
hgdprs758724746
ensemblrs758724746
geneviewrs758724746
scholarrs758724746
googlers758724746
pharmgkbrs758724746
gwascentralrs758724746
openSNPrs758724746
23andMers758724746
SNPshotrs758724746
SNPdbers758724746
MSV3drs758724746
GWAS Ctlgrs758724746
Max Magnitude0
ClinVar
Risk rs758724746(A;A)
Alt rs758724746(A;A)
Reference Rs758724746(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CPS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.211473231G>A
CLNSRC
CLNACC RCV000414131.1,