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rs6679667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6679667(C;C)
Make rs6679667(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position105113603
is asnp
is mentioned by
dbSNPrs6679667
ebirs6679667
HLIrs6679667
Exacrs6679667
Varsomers6679667
Maprs6679667
PheGenIrs6679667
hapmaprs6679667
1000 genomesrs6679667
hgdprs6679667
ensemblrs6679667
gopubmedrs6679667
geneviewrs6679667
scholarrs6679667
googlers6679667
pharmgkbrs6679667
gwascentralrs6679667
openSNPrs6679667
23andMers6679667
23andMe allrs6679667
SNP Nexus

SNPshotrs6679667
SNPdbers6679667
MSV3drs6679667
GWAS Ctlgrs6679667
Max Magnitude0
rs6679667 is a SNP in the PTPN22 gene, found to be perfectly correlated with SNP rs2476601, a SNP associated with many autoimmune diseases. [PMID 17554300OA-icon.png]
OMIM600716
DescPROTEIN TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 22; PTPN22
Variant
Relatedalso