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rs1712790

From SNPedia

Orientationplus
Stabilizedplus
Make rs1712790(C;C)
Make rs1712790(C;T)
Make rs1712790(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position114750747
is asnp
is mentioned by
dbSNPrs1712790
ebirs1712790
HLIrs1712790
Exacrs1712790
Varsomers1712790
Maprs1712790
PheGenIrs1712790
hapmaprs1712790
1000 genomesrs1712790
hgdprs1712790
ensemblrs1712790
gopubmedrs1712790
geneviewrs1712790
scholarrs1712790
googlers1712790
pharmgkbrs1712790
gwascentralrs1712790
openSNPrs1712790
23andMers1712790
23andMe allrs1712790
SNP Nexus

SNPshotrs1712790
SNPdbers1712790
MSV3drs1712790
GWAS Ctlgrs1712790
GMAF0.4063
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs1712790
PubMedID [PMID 17903292OA-icon.png]
Condition Urinary albumin excretion
Gene FAM55B
Risk Allele
pValue 2.00E-006
OR NA
95% CI



GET Evidence
rs1712790
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary