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rs17179670

From SNPedia

Orientationplus
Stabilizedplus
Make rs17179670(A;A)
Make rs17179670(A;G)
Make rs17179670(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position65956032
GeneHMGA2
is asnp
is mentioned by
dbSNPrs17179670
dbSNP (classic)rs17179670
ClinGenrs17179670
ebirs17179670
HLIrs17179670
Exacrs17179670
Gnomadrs17179670
Varsomers17179670
LitVarrs17179670
Maprs17179670
PheGenIrs17179670
Biobankrs17179670
1000 genomesrs17179670
hgdprs17179670
ensemblrs17179670
geneviewrs17179670
scholarrs17179670
googlers17179670
pharmgkbrs17179670
gwascentralrs17179670
openSNPrs17179670
23andMers17179670
SNPshotrs17179670
SNPdbers17179670
MSV3drs17179670
GWAS Ctlgrs17179670
GMAF0.1309
Max Magnitude0
? (A;A) (A;G) (G;G) 28


Rs17179670 is a SNP implicated in Tooth Development


[PMID 21358824OA-icon.png] Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans.