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rs6063312

From SNPedia

Orientationplus
Stabilizedplus
Make rs6063312(G;G)
Make rs6063312(G;T)
Make rs6063312(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position48726522
GenePREX1
is asnp
is mentioned by
dbSNPrs6063312
ebirs6063312
HLIrs6063312
Exacrs6063312
Varsomers6063312
Maprs6063312
PheGenIrs6063312
hapmaprs6063312
1000 genomesrs6063312
hgdprs6063312
ensemblrs6063312
gopubmedrs6063312
geneviewrs6063312
scholarrs6063312
googlers6063312
pharmgkbrs6063312
gwascentralrs6063312
openSNPrs6063312
23andMers6063312
23andMe allrs6063312
SNP Nexus

SNPshotrs6063312
SNPdbers6063312
MSV3drs6063312
GWAS Ctlgrs6063312
GMAF0.1612
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs6063312
PubMedID [PMID 17903302OA-icon.png]
Condition Tonometry
Gene PREX1
Risk Allele
pValue 2.00E-006
OR NA
95% CI



GET Evidence
rs6063312
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary