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rs6845865

From SNPedia

Orientationplus
Stabilizedplus
Make rs6845865(C;C)
Make rs6845865(C;T)
Make rs6845865(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position148053451
GeneARHGAP10
is asnp
is mentioned by
dbSNPrs6845865
ebirs6845865
HLIrs6845865
Exacrs6845865
Varsomers6845865
Maprs6845865
PheGenIrs6845865
hapmaprs6845865
1000 genomesrs6845865
hgdprs6845865
ensemblrs6845865
gopubmedrs6845865
geneviewrs6845865
scholarrs6845865
googlers6845865
pharmgkbrs6845865
gwascentralrs6845865
openSNPrs6845865
23andMers6845865
23andMe allrs6845865
SNP Nexus

SNPshotrs6845865
SNPdbers6845865
MSV3drs6845865
GWAS Ctlgrs6845865
GMAF0.2466
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait QT interval
Title A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations: The EUROSPAN Project
Risk Allele G
P-val 7E-7
Odds Ratio 0.19 [0.11-0.27] unit increase


GET Evidence
rs6845865
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.34375
summary