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rs991316

From SNPedia

Orientationminus
Stabilizedminus
Make rs991316(A;A)
Make rs991316(A;G)
Make rs991316(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position99401288
GeneLOC102723576
is asnp
is mentioned by
dbSNPrs991316
ebirs991316
HLIrs991316
Exacrs991316
Varsomers991316
Maprs991316
PheGenIrs991316
hapmaprs991316
1000 genomesrs991316
hgdprs991316
ensemblrs991316
gopubmedrs991316
geneviewrs991316
scholarrs991316
googlers991316
pharmgkbrs991316
gwascentralrs991316
openSNPrs991316
23andMers991316
23andMe allrs991316
SNP Nexus

SNPshotrs991316
SNPdbers991316
MSV3drs991316
GWAS Ctlgrs991316
GMAF0.3967
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19609347OA-icon.png]
Trait Hypertension
Title A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans
Risk Allele T
P-val 0.000005
Odds Ratio 1.62 [NR]


[PMID 22662130OA-icon.png] Using Prior Information from the Medical Literature in GWAS of Oral Cancer Identifies Novel Susceptibility Variant on Chromosome 4 - the AdAPT Method


[PMID 19176549OA-icon.png] Genome-wide association analysis by lasso penalized logistic regression.


GET Evidence
rs991316
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary