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rs1722146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1722146(C;C)
Make rs1722146(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position46032946
is asnp
is mentioned by
dbSNPrs1722146
ebirs1722146
HLIrs1722146
Exacrs1722146
Varsomers1722146
Maprs1722146
PheGenIrs1722146
hapmaprs1722146
1000 genomesrs1722146
hgdprs1722146
ensemblrs1722146
gopubmedrs1722146
geneviewrs1722146
scholarrs1722146
googlers1722146
pharmgkbrs1722146
gwascentralrs1722146
openSNPrs1722146
23andMers1722146
23andMe allrs1722146
SNP Nexus

SNPshotrs1722146
SNPdbers1722146
MSV3drs1722146
GWAS Ctlgrs1722146
GMAF0.14
Max Magnitude0
? (C;C) (C;T) (T;T) 28