Have questions? Visit https://www.reddit.com/r/SNPedia

rs17695937

From SNPedia

Orientationplus
Stabilizedplus
Make rs17695937(A;A)
Make rs17695937(A;G)
Make rs17695937(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position97711412
is asnp
is mentioned by
dbSNPrs17695937
ebirs17695937
HLIrs17695937
Exacrs17695937
Varsomers17695937
Maprs17695937
PheGenIrs17695937
hapmaprs17695937
1000 genomesrs17695937
hgdprs17695937
ensemblrs17695937
gopubmedrs17695937
geneviewrs17695937
scholarrs17695937
googlers17695937
pharmgkbrs17695937
gwascentralrs17695937
openSNPrs17695937
23andMers17695937
23andMe allrs17695937
SNP Nexus

SNPshotrs17695937
SNPdbers17695937
MSV3drs17695937
GWAS Ctlgrs17695937
GMAF0.1602
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24103478] Contribution of PTPN22, CD28, CTLA-4 and ZAP-70 variants to the risk of type 1 diabetes in Tunisians


[PMID 23406209] Association of ZAP70 and PTPN6, but Not BANK1 or CLEC2D, with inflammatory bowel disease in the Tunisian population.