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rs337663

From SNPedia

Orientationplus
Stabilizedplus
Make rs337663(A;A)
Make rs337663(A;G)
Make rs337663(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position92311428
is asnp
is mentioned by
dbSNPrs337663
ebirs337663
HLIrs337663
Exacrs337663
Varsomers337663
Maprs337663
PheGenIrs337663
hapmaprs337663
1000 genomesrs337663
hgdprs337663
ensemblrs337663
gopubmedrs337663
geneviewrs337663
scholarrs337663
googlers337663
pharmgkbrs337663
gwascentralrs337663
openSNPrs337663
23andMers337663
23andMe allrs337663
SNP Nexus

SNPshotrs337663
SNPdbers337663
MSV3drs337663
GWAS Ctlgrs337663
GMAF0.4031
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19324860OA-icon.png] An international collaborative family-based whole-genome linkage scan for high-grade myopia


[PMID 18323491OA-icon.png] Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study.


[PMID 19001172OA-icon.png] Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci.