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rs7745040

From SNPedia

Orientationplus
Stabilizedplus
Make rs7745040(C;C)
Make rs7745040(C;T)
Make rs7745040(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32696555
is asnp
is mentioned by
dbSNPrs7745040
ebirs7745040
HLIrs7745040
Exacrs7745040
Varsomers7745040
Maprs7745040
PheGenIrs7745040
hapmaprs7745040
1000 genomesrs7745040
hgdprs7745040
ensemblrs7745040
gopubmedrs7745040
geneviewrs7745040
scholarrs7745040
googlers7745040
pharmgkbrs7745040
gwascentralrs7745040
openSNPrs7745040
23andMers7745040
23andMe allrs7745040
SNP Nexus

SNPshotrs7745040
SNPdbers7745040
MSV3drs7745040
GWAS Ctlgrs7745040
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24776925OA-icon.png] Whole-exome sequencing for the identification of susceptibility genes of kashin-beck disease