Have questions? Visit https://www.reddit.com/r/SNPedia

rs17104630

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17104630(A;G)
Make rs17104630(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position36530844
is asnp
is mentioned by
dbSNPrs17104630
ebirs17104630
HLIrs17104630
Exacrs17104630
Varsomers17104630
Maprs17104630
PheGenIrs17104630
hapmaprs17104630
1000 genomesrs17104630
hgdprs17104630
ensemblrs17104630
gopubmedrs17104630
geneviewrs17104630
scholarrs17104630
googlers17104630
pharmgkbrs17104630
gwascentralrs17104630
openSNPrs17104630
23andMers17104630
23andMe allrs17104630
SNP Nexus

SNPshotrs17104630
SNPdbers17104630
MSV3drs17104630
GWAS Ctlgrs17104630
GMAF0.09688
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391950OA-icon.png]
Trait Height
Title Identification of ten loci associated with height highlights new biological pathways in human growth
Risk Allele G
P-val 0.0000079999999999999996
Odds Ratio 0.42 [0.61-1.10] cm shorter


GET Evidence
rs17104630
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0546875
summary