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rs5017717

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs5017717(C;T)
Make rs5017717(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position93884869
GenePROS1
is asnp
is mentioned by
dbSNPrs5017717
ebirs5017717
HLIrs5017717
Exacrs5017717
Varsomers5017717
Maprs5017717
PheGenIrs5017717
hapmaprs5017717
1000 genomesrs5017717
hgdprs5017717
ensemblrs5017717
gopubmedrs5017717
geneviewrs5017717
scholarrs5017717
googlers5017717
pharmgkbrs5017717
gwascentralrs5017717
openSNPrs5017717
23andMers5017717
23andMe allrs5017717
SNP Nexus

SNPshotrs5017717
SNPdbers5017717
MSV3drs5017717
GWAS Ctlgrs5017717
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs5017717(T;T)
Alt rs5017717(T;T)
Reference rs5017717(C;C)
Significance Untested
Disease
Variation info
Gene PROS1
CLNDBN OMIM
Reversed 1
HGVS NC_000003.11:g.93603713G>A
CLNSRC
CLNACC