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rs7990916

From SNPedia

Orientationplus
Stabilizedplus
Make rs7990916(C;C)
Make rs7990916(C;T)
Make rs7990916(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position80065389
is asnp
is mentioned by
dbSNPrs7990916
ebirs7990916
HLIrs7990916
Exacrs7990916
Varsomers7990916
Maprs7990916
PheGenIrs7990916
hapmaprs7990916
1000 genomesrs7990916
hgdprs7990916
ensemblrs7990916
gopubmedrs7990916
geneviewrs7990916
scholarrs7990916
googlers7990916
pharmgkbrs7990916
gwascentralrs7990916
openSNPrs7990916
23andMers7990916
23andMe allrs7990916
SNP Nexus

SNPshotrs7990916
SNPdbers7990916
MSV3drs7990916
GWAS Ctlgrs7990916
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25019275] Lack of association of a genetic variant in the long intergenic noncoding RNA (linc01080) with Alzheimer's disease and amnestic mild cognitive impairment in Han Chinese