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rs7778619

From SNPedia

Orientationplus
Stabilizedplus
Make rs7778619(C;C)
Make rs7778619(C;G)
Make rs7778619(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position10110349
GeneLOC340268
is asnp
is mentioned by
dbSNPrs7778619
ebirs7778619
HLIrs7778619
Exacrs7778619
Varsomers7778619
Maprs7778619
PheGenIrs7778619
hapmaprs7778619
1000 genomesrs7778619
hgdprs7778619
ensemblrs7778619
gopubmedrs7778619
geneviewrs7778619
scholarrs7778619
googlers7778619
pharmgkbrs7778619
gwascentralrs7778619
openSNPrs7778619
23andMers7778619
23andMe allrs7778619
SNP Nexus

SNPshotrs7778619
SNPdbers7778619
MSV3drs7778619
GWAS Ctlgrs7778619
GMAF0.2938
Max Magnitude
? (C;C) (C;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 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs7778619
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary