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rs1049225

From SNPedia

Orientationminus
Stabilizedminus
Make rs1049225(C;C)
Make rs1049225(C;T)
Make rs1049225(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position32659970
is asnp
is mentioned by
dbSNPrs1049225
ebirs1049225
HLIrs1049225
Exacrs1049225
Varsomers1049225
Maprs1049225
PheGenIrs1049225
hapmaprs1049225
1000 genomesrs1049225
hgdprs1049225
ensemblrs1049225
gopubmedrs1049225
geneviewrs1049225
scholarrs1049225
googlers1049225
pharmgkbrs1049225
gwascentralrs1049225
openSNPrs1049225
23andMers1049225
23andMe allrs1049225
SNP Nexus

SNPshotrs1049225
SNPdbers1049225
MSV3drs1049225
GWAS Ctlgrs1049225
Max Magnitude
778 Common variable immunodeficiency disorder (CVID) cases compared with 10,999 controls using the Illumina Immunochip; confirming the previously reported human leukocyte antigen (HLA) associations on chromosome 6p21. The minor allele, rs1049225(T) as represented on the minus strand, is associated with reduced risk for CVID (odds ratio 0.56, CI: 0.49 - 0.64, p=4.8 × 10e-16).[PMID 25891430OA-icon.png]