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rs17736767

From SNPedia

Orientationplus
Stabilizedplus
Make rs17736767(C;C)
Make rs17736767(C;G)
Make rs17736767(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position99244260
is asnp
is mentioned by
dbSNPrs17736767
dbSNP (classic)rs17736767
ClinGenrs17736767
ebirs17736767
HLIrs17736767
Exacrs17736767
Gnomadrs17736767
Varsomers17736767
LitVarrs17736767
Maprs17736767
PheGenIrs17736767
Biobankrs17736767
1000 genomesrs17736767
hgdprs17736767
ensemblrs17736767
geneviewrs17736767
scholarrs17736767
googlers17736767
pharmgkbrs17736767
gwascentralrs17736767
openSNPrs17736767
23andMers17736767
SNPshotrs17736767
SNPdbers17736767
MSV3drs17736767
GWAS Ctlgrs17736767
GMAF0.1905
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 22044751OA-icon.png]
Trait
Title Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.
Risk Allele G
P-val 0.000007
Odds Ratio 0.2080 None