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rs3769048

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3769048(C;T)
Make rs3769048(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position237861218
GeneRAMP1
is asnp
is mentioned by
dbSNPrs3769048
ebirs3769048
HLIrs3769048
Exacrs3769048
Varsomers3769048
Maprs3769048
PheGenIrs3769048
hapmaprs3769048
1000 genomesrs3769048
hgdprs3769048
ensemblrs3769048
gopubmedrs3769048
geneviewrs3769048
scholarrs3769048
googlers3769048
pharmgkbrs3769048
gwascentralrs3769048
openSNPrs3769048
23andMers3769048
23andMe allrs3769048
SNP Nexus

SNPshotrs3769048
SNPdbers3769048
MSV3drs3769048
GWAS Ctlgrs3769048
GMAF0.07759
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19710695] Haplotype-based case-control study of receptor (calcitonin) activity-modifying protein-1 gene in cerebral infarction