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rs3737002

From SNPedia

Orientationplus
Stabilizedplus
Make rs3737002(C;C)
Make rs3737002(C;T)
Make rs3737002(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position207587428
GeneCR1
is asnp
is mentioned by
dbSNPrs3737002
dbSNP (classic)rs3737002
ClinGenrs3737002
ebirs3737002
HLIrs3737002
Exacrs3737002
Gnomadrs3737002
Varsomers3737002
LitVarrs3737002
Maprs3737002
PheGenIrs3737002
Biobankrs3737002
1000 genomesrs3737002
hgdprs3737002
ensemblrs3737002
geneviewrs3737002
scholarrs3737002
googlers3737002
pharmgkbrs3737002
gwascentralrs3737002
openSNPrs3737002
23andMers3737002
SNPshotrs3737002
SNPdbers3737002
MSV3drs3737002
GWAS Ctlgrs3737002
GMAF0.2658
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24018213] Missense variants in CR1 are associated with increased risk of Alzheimer' disease in Han Chinese


[PMID 29920840] Targeted resequencing reveals genetic risks in patients with sporadic idiopathic pulmonary fibrosis.