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rs10777332

From SNPedia

Orientationplus
Stabilizedplus
Make rs10777332(C;C)
Make rs10777332(C;T)
Make rs10777332(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position91770525
is asnp
is mentioned by
dbSNPrs10777332
ebirs10777332
HLIrs10777332
Exacrs10777332
Varsomers10777332
Maprs10777332
PheGenIrs10777332
hapmaprs10777332
1000 genomesrs10777332
hgdprs10777332
ensemblrs10777332
gopubmedrs10777332
geneviewrs10777332
scholarrs10777332
googlers10777332
pharmgkbrs10777332
gwascentralrs10777332
openSNPrs10777332
23andMers10777332
23andMe allrs10777332
SNP Nexus

SNPshotrs10777332
SNPdbers10777332
MSV3drs10777332
GWAS Ctlgrs10777332
GMAF0.1878
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19260141OA-icon.png]
Trait Biochemical measures
Title Genome-wide association study of biochemical traits in Korcula Island, Croatia
Risk Allele A
P-val 0.000005
Odds Ratio 0.24 [0.14-0.34] mmol/L decrease
[PMID 19260141OA-icon.png] gwas among adults residing on Korcula Island in Croatia, cholesterol, the A allele associated with decreased total cholesterol levels



GET Evidence
rs10777332
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary