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rs5742915

From SNPedia

Orientationplus
Stabilizedplus
Make rs5742915(C;C)
Make rs5742915(C;T)
Make rs5742915(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position74044292
GenePML
is asnp
is mentioned by
dbSNPrs5742915
ebirs5742915
HLIrs5742915
Exacrs5742915
Varsomers5742915
Maprs5742915
PheGenIrs5742915
hapmaprs5742915
1000 genomesrs5742915
hgdprs5742915
ensemblrs5742915
gopubmedrs5742915
geneviewrs5742915
scholarrs5742915
googlers5742915
pharmgkbrs5742915
gwascentralrs5742915
openSNPrs5742915
23andMers5742915
23andMe allrs5742915
SNP Nexus

SNPshotrs5742915
SNPdbers5742915
MSV3drs5742915
GWAS Ctlgrs5742915
GMAF0.2268
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height
Risk Allele T
P-val 5E-7
Odds Ratio 0.03 [NR] unit decrease
GWAS snp
PMID [PMID 21623375]
Trait
Title Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Risk Allele C
P-val 2E-14
Odds Ratio 1.3400 [1.25-1.45]


GET Evidence
PML-F645L
aa_change Phe645Leu
aa_change_short F645L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.337609
summary