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rs2070488

From SNPedia

Orientationplus
Stabilizedplus
Make rs2070488(A;A)
Make rs2070488(A;G)
Make rs2070488(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38400999
GeneXYLB
is asnp
is mentioned by
dbSNPrs2070488
ebirs2070488
HLIrs2070488
Exacrs2070488
Varsomers2070488
Maprs2070488
PheGenIrs2070488
hapmaprs2070488
1000 genomesrs2070488
hgdprs2070488
ensemblrs2070488
gopubmedrs2070488
geneviewrs2070488
scholarrs2070488
googlers2070488
pharmgkbrs2070488
gwascentralrs2070488
openSNPrs2070488
23andMers2070488
23andMe allrs2070488
SNP Nexus

SNPshotrs2070488
SNPdbers2070488
MSV3drs2070488
GWAS Ctlgrs2070488
GMAF0.3609
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19389651OA-icon.png]
Trait Electrocardiographic conduction measures
Title Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae
Risk Allele A
P-val 0.000004
Odds Ratio 5.00 [2.84-7.16] ms decrease


GET Evidence
rs2070488
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.439952
summary