Rs1395479

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Orientationplus
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ReferenceGRCh38 38.1/141
Chromosome4
Position177397037
is asnp
is mentioned by
dbSNPrs1395479
Exacrs1395479
PheGenIrs1395479
nextbiors1395479
hapmaprs1395479
1000 genomesrs1395479
hgdprs1395479
ensemblrs1395479
gopubmedrs1395479
geneviewrs1395479
scholarrs1395479
googlers1395479
pharmgkbrs1395479
gwascentralrs1395479
openSNPrs1395479
23andMers1395479
23andMe allrs1395479
SNP Nexus

SNPshotrs1395479
SNPdbers1395479
MSV3drs1395479
GMAF0.1882
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs1395479
PubMedID [PMID 17903306OA-icon.png]
Condition Heart rate variability traits
Gene NEIL3
Risk Allele
pValue 7.00E-006
OR NA
95% CI



GET Evidence
rs1395479
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary



GWAS snp
PMID [PMID 23698163OA-icon.png]
Trait Serum selenium levels
Title Genome-wide association study of serum selenium concentrations.
Risk Allele A
P-val 3E-7
Odds Ratio .04 [0.027-0.059] mg/dL increase