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rs7093146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7093146(C;C)
Make rs7093146(C;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position123367880
is asnp
is mentioned by
dbSNPrs7093146
ebirs7093146
HLIrs7093146
Exacrs7093146
Varsomers7093146
Maprs7093146
PheGenIrs7093146
hapmaprs7093146
1000 genomesrs7093146
hgdprs7093146
ensemblrs7093146
gopubmedrs7093146
geneviewrs7093146
scholarrs7093146
googlers7093146
pharmgkbrs7093146
gwascentralrs7093146
openSNPrs7093146
23andMers7093146
23andMe allrs7093146
SNP Nexus

SNPshotrs7093146
SNPdbers7093146
MSV3drs7093146
GWAS Ctlgrs7093146
GMAF0.1235
Max Magnitude0
OMIM602228
DescTRANSCRIPTION FACTOR 7-LIKE 2; TCF7L2
Variant
Relatedalso