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rs10199956

From SNPedia

Orientationplus
Stabilizedplus
Make rs10199956(G;G)
Make rs10199956(G;T)
Make rs10199956(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position237907946
GeneRAMP1
is asnp
is mentioned by
dbSNPrs10199956
ebirs10199956
HLIrs10199956
Exacrs10199956
Varsomers10199956
Maprs10199956
PheGenIrs10199956
hapmaprs10199956
1000 genomesrs10199956
hgdprs10199956
ensemblrs10199956
gopubmedrs10199956
geneviewrs10199956
scholarrs10199956
googlers10199956
pharmgkbrs10199956
gwascentralrs10199956
openSNPrs10199956
23andMers10199956
23andMe allrs10199956
SNP Nexus

SNPshotrs10199956
SNPdbers10199956
MSV3drs10199956
GWAS Ctlgrs10199956
GMAF0.4426
Max Magnitude
? (G;G) (G;T) (T;T) 28

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