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rs13375391

From SNPedia

Orientationplus
Stabilizedplus
Make rs13375391(A;A)
Make rs13375391(A;G)
Make rs13375391(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position185825751
GeneHMCN1
is asnp
is mentioned by
dbSNPrs13375391
dbSNP (classic)rs13375391
ClinGenrs13375391
ebirs13375391
HLIrs13375391
Exacrs13375391
Gnomadrs13375391
Varsomers13375391
LitVarrs13375391
Maprs13375391
PheGenIrs13375391
Biobankrs13375391
1000 genomesrs13375391
hgdprs13375391
ensemblrs13375391
geneviewrs13375391
scholarrs13375391
googlers13375391
pharmgkbrs13375391
gwascentralrs13375391
openSNPrs13375391
23andMers13375391
SNPshotrs13375391
SNPdbers13375391
MSV3drs13375391
GWAS Ctlgrs13375391
GMAF0.01699
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23534349OA-icon.png]
Trait QRS duration
Title Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
Risk Allele A
P-val 9E-6
Odds Ratio 5.82 [NR] ms increase