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rs6599001

From SNPedia

Orientationplus
Make rs6599001(C;C)
Make rs6599001(C;T)
Make rs6599001(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position39032660
GeneLOC105377643
is asnp
is mentioned by
dbSNPrs6599001
ebirs6599001
HLIrs6599001
Exacrs6599001
Varsomers6599001
Maprs6599001
PheGenIrs6599001
hapmaprs6599001
1000 genomesrs6599001
hgdprs6599001
ensemblrs6599001
gopubmedrs6599001
geneviewrs6599001
scholarrs6599001
googlers6599001
pharmgkbrs6599001
gwascentralrs6599001
openSNPrs6599001
23andMers6599001
23andMe allrs6599001
SNP Nexus

SNPshotrs6599001
SNPdbers6599001
MSV3drs6599001
GWAS Ctlgrs6599001
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26186006OA-icon.png] Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal