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rs10516541

From SNPedia

Orientationplus
Stabilizedplus
Make rs10516541(A;A)
Make rs10516541(A;G)
Make rs10516541(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position107194065
is asnp
is mentioned by
dbSNPrs10516541
ebirs10516541
HLIrs10516541
Exacrs10516541
Varsomers10516541
Maprs10516541
PheGenIrs10516541
hapmaprs10516541
1000 genomesrs10516541
hgdprs10516541
ensemblrs10516541
gopubmedrs10516541
geneviewrs10516541
scholarrs10516541
googlers10516541
pharmgkbrs10516541
gwascentralrs10516541
openSNPrs10516541
23andMers10516541
23andMe allrs10516541
SNP Nexus

SNPshotrs10516541
SNPdbers10516541
MSV3drs10516541
GWAS Ctlgrs10516541
GMAF0.3085
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs10516541
PubMedID [PMID 17903307OA-icon.png]
Condition Mean forced vital capacity from 2 exams
Gene Intergenic
Risk Allele
pValue 4.00E-006
OR NA
95% CI



[PMID 17903293OA-icon.png] Genome-wide association with select biomarker traits in the Framingham Heart Study.


GET Evidence
rs10516541
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.328125
summary