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rs10759944

From SNPedia

Orientationplus
Stabilizedplus
Make rs10759944(A;A)
Make rs10759944(A;G)
Make rs10759944(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position97794690
is asnp
is mentioned by
dbSNPrs10759944
ebirs10759944
HLIrs10759944
Exacrs10759944
Varsomers10759944
Maprs10759944
PheGenIrs10759944
hapmaprs10759944
1000 genomesrs10759944
hgdprs10759944
ensemblrs10759944
gopubmedrs10759944
geneviewrs10759944
scholarrs10759944
googlers10759944
pharmgkbrs10759944
gwascentralrs10759944
openSNPrs10759944
23andMers10759944
23andMe allrs10759944
SNP Nexus

SNPshotrs10759944
SNPdbers10759944
MSV3drs10759944
GWAS Ctlgrs10759944
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25918370OA-icon.png] Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer