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rs1998303

From SNPedia

Orientationplus
Stabilizedplus
Make rs1998303(A;A)
Make rs1998303(A;G)
Make rs1998303(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position82800066
is asnp
is mentioned by
dbSNPrs1998303
ebirs1998303
HLIrs1998303
Exacrs1998303
Varsomers1998303
Maprs1998303
PheGenIrs1998303
hapmaprs1998303
1000 genomesrs1998303
hgdprs1998303
ensemblrs1998303
gopubmedrs1998303
geneviewrs1998303
scholarrs1998303
googlers1998303
pharmgkbrs1998303
gwascentralrs1998303
openSNPrs1998303
23andMers1998303
23andMe allrs1998303
SNP Nexus

SNPshotrs1998303
SNPdbers1998303
MSV3drs1998303
GWAS Ctlgrs1998303
GMAF0.3939
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR


GET Evidence
rs1998303
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359375
summary