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rs10893872

From SNPedia

Orientationplus
Stabilizedplus
Make rs10893872(C;C)
Make rs10893872(C;T)
Make rs10893872(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position128455658
is asnp
is mentioned by
dbSNPrs10893872
ebirs10893872
HLIrs10893872
Exacrs10893872
Varsomers10893872
Maprs10893872
PheGenIrs10893872
hapmaprs10893872
1000 genomesrs10893872
hgdprs10893872
ensemblrs10893872
gopubmedrs10893872
geneviewrs10893872
scholarrs10893872
googlers10893872
pharmgkbrs10893872
gwascentralrs10893872
openSNPrs10893872
23andMers10893872
23andMe allrs10893872
SNP Nexus

SNPshotrs10893872
SNPdbers10893872
MSV3drs10893872
GWAS Ctlgrs10893872
GMAF0.4247
Max Magnitude
? (C;C) (C;T) (T;T) 28

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[PMID 20169177OA-icon.png] Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.


[PMID 26241881] Association of E26 Transformation Specific Sequence 1 Variants with Rheumatoid Arthritis in Chinese Han Population