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rs8106822

From SNPedia

Orientationplus
Stabilizedplus
Make rs8106822(A;A)
Make rs8106822(A;G)
Make rs8106822(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position31373516
is asnp
is mentioned by
dbSNPrs8106822
ebirs8106822
HLIrs8106822
Exacrs8106822
Varsomers8106822
Maprs8106822
PheGenIrs8106822
hapmaprs8106822
1000 genomesrs8106822
hgdprs8106822
ensemblrs8106822
gopubmedrs8106822
geneviewrs8106822
scholarrs8106822
googlers8106822
pharmgkbrs8106822
gwascentralrs8106822
openSNPrs8106822
23andMers8106822
23andMe allrs8106822
SNP Nexus

SNPshotrs8106822
SNPdbers8106822
MSV3drs8106822
GWAS Ctlgrs8106822
GMAF0.4582
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19808960OA-icon.png] Apolipoprotein E/C1 Locus Variants Modify Renal Cell Carcinoma Risk