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rs757205958

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757205958(A;A)
Make rs757205958(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position210605178
GeneCPS1
is asnp
is mentioned by
dbSNPrs757205958
ebirs757205958
HLIrs757205958
Exacrs757205958
Varsomers757205958
Maprs757205958
PheGenIrs757205958
hapmaprs757205958
1000 genomesrs757205958
hgdprs757205958
ensemblrs757205958
gopubmedrs757205958
geneviewrs757205958
scholarrs757205958
googlers757205958
pharmgkbrs757205958
gwascentralrs757205958
openSNPrs757205958
23andMers757205958
23andMe allrs757205958
SNP Nexus

SNPshotrs757205958
SNPdbers757205958
MSV3drs757205958
GWAS Ctlgrs757205958
Max Magnitude0
ClinVar
Risk rs757205958(A,C;A,C)
Alt rs757205958(A,C;A,C)
Reference rs757205958(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CPS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.211469902G>C
CLNSRC
CLNACC RCV000185818.1,