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rs9305354

From SNPedia

Orientationplus
Stabilizedplus
Make rs9305354(C;C)
Make rs9305354(C;T)
Make rs9305354(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position28102877
GeneLINC00473
is asnp
is mentioned by
dbSNPrs9305354
ebirs9305354
HLIrs9305354
Exacrs9305354
Varsomers9305354
Maprs9305354
PheGenIrs9305354
hapmaprs9305354
1000 genomesrs9305354
hgdprs9305354
ensemblrs9305354
gopubmedrs9305354
geneviewrs9305354
scholarrs9305354
googlers9305354
pharmgkbrs9305354
gwascentralrs9305354
openSNPrs9305354
23andMers9305354
23andMe allrs9305354
SNP Nexus

SNPshotrs9305354
SNPdbers9305354
MSV3drs9305354
GWAS Ctlgrs9305354
GMAF0.298
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903292OA-icon.png]
Trait Urinary albumin excretion
Title A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study
Risk Allele
P-val 0.0000079999999999999996
Odds Ratio NR NR


GET Evidence
rs9305354
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.34375
summary