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rs1035127

From SNPedia

Orientationminus
Make rs1035127(C;C)
Make rs1035127(C;T)
Make rs1035127(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position102403459
is asnp
is mentioned by
dbSNPrs1035127
ebirs1035127
HLIrs1035127
Exacrs1035127
Varsomers1035127
Maprs1035127
PheGenIrs1035127
hapmaprs1035127
1000 genomesrs1035127
hgdprs1035127
ensemblrs1035127
gopubmedrs1035127
geneviewrs1035127
scholarrs1035127
googlers1035127
pharmgkbrs1035127
gwascentralrs1035127
openSNPrs1035127
23andMers1035127
23andMe allrs1035127
SNP Nexus

SNPshotrs1035127
SNPdbers1035127
MSV3drs1035127
GWAS Ctlgrs1035127
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26566691] Polymorphisms of ST2-IL18R1-IL18RAP gene cluster: a new risk for autoimmune thyroid diseases