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rs17144046

From SNPedia

Orientationplus
Stabilizedplus
Make rs17144046(A;A)
Make rs17144046(A;G)
Make rs17144046(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position8564051
is asnp
is mentioned by
dbSNPrs17144046
dbSNP (old)rs17144046
ClinGenrs17144046
ebirs17144046
HLIrs17144046
Exacrs17144046
Gnomadrs17144046
Varsomers17144046
Maprs17144046
PheGenIrs17144046
Biobankrs17144046
1000 genomesrs17144046
hgdprs17144046
ensemblrs17144046
gopubmedrs17144046
geneviewrs17144046
scholarrs17144046
googlers17144046
pharmgkbrs17144046
gwascentralrs17144046
openSNPrs17144046
23andMers17144046
23andMe allrs17144046
SNPshotrs17144046
SNPdbers17144046
MSV3drs17144046
GWAS Ctlgrs17144046
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 28656603] A genetic variant near GATA3 implicated in inherited susceptibility and etiology of benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS).