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rs7527798

From SNPedia

Orientationplus
Stabilizedplus
Make rs7527798(C;C)
Make rs7527798(C;T)
Make rs7527798(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position207698945
GeneCR1L
is asnp
is mentioned by
dbSNPrs7527798
ebirs7527798
HLIrs7527798
Exacrs7527798
Varsomers7527798
Maprs7527798
PheGenIrs7527798
hapmaprs7527798
1000 genomesrs7527798
hgdprs7527798
ensemblrs7527798
gopubmedrs7527798
geneviewrs7527798
scholarrs7527798
googlers7527798
pharmgkbrs7527798
gwascentralrs7527798
openSNPrs7527798
23andMers7527798
23andMe allrs7527798
SNP Nexus

SNPshotrs7527798
SNPdbers7527798
MSV3drs7527798
GWAS Ctlgrs7527798
GMAF0.141
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21700265OA-icon.png]
Trait
Title Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.
Risk Allele
P-val 2E-9
Odds Ratio 0.1000 [NR] unit increase


[PMID 22430674OA-icon.png] Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.


[PMID 23856853OA-icon.png] Association of a complement receptor 1 gene variant with baseline erythrocyte sedimentation rate levels in patients starting anti-TNF therapy in a UK rheumatoid arthritis cohort: results from the Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate cohort.