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rs4965598

From SNPedia

Orientationplus
Stabilizedplus
Make rs4965598(C;C)
Make rs4965598(C;T)
Make rs4965598(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position100219409
GeneADAMTS17
is asnp
is mentioned by
dbSNPrs4965598
ebirs4965598
HLIrs4965598
Exacrs4965598
Varsomers4965598
Maprs4965598
PheGenIrs4965598
hapmaprs4965598
1000 genomesrs4965598
hgdprs4965598
ensemblrs4965598
gopubmedrs4965598
geneviewrs4965598
scholarrs4965598
googlers4965598
pharmgkbrs4965598
gwascentralrs4965598
openSNPrs4965598
23andMers4965598
23andMe allrs4965598
SNP Nexus

SNPshotrs4965598
SNPdbers4965598
MSV3drs4965598
GWAS Ctlgrs4965598
GMAF0.236
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 4E-13
Odds Ratio .03 [NR] unit decrease