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rs7996217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7996217(G;G)
Make rs7996217(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position101348594
GeneNALCN
is asnp
is mentioned by
dbSNPrs7996217
ebirs7996217
HLIrs7996217
Exacrs7996217
Varsomers7996217
Maprs7996217
PheGenIrs7996217
hapmaprs7996217
1000 genomesrs7996217
hgdprs7996217
ensemblrs7996217
gopubmedrs7996217
geneviewrs7996217
scholarrs7996217
googlers7996217
pharmgkbrs7996217
gwascentralrs7996217
openSNPrs7996217
23andMers7996217
23andMe allrs7996217
SNP Nexus

SNPshotrs7996217
SNPdbers7996217
MSV3drs7996217
GWAS Ctlgrs7996217
GMAF0.01148
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22628157OA-icon.png]
Trait
Title Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.
Risk Allele T
P-val 7E-7
Odds Ratio None None