Have questions? Visit https://www.reddit.com/r/SNPedia

rs6582584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs6582584(C;C)
Make rs6582584(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position38318340
GeneALG10B
is asnp
is mentioned by
dbSNPrs6582584
ebirs6582584
HLIrs6582584
Exacrs6582584
Varsomers6582584
Maprs6582584
PheGenIrs6582584
hapmaprs6582584
1000 genomesrs6582584
hgdprs6582584
ensemblrs6582584
gopubmedrs6582584
geneviewrs6582584
scholarrs6582584
googlers6582584
pharmgkbrs6582584
gwascentralrs6582584
openSNPrs6582584
23andMers6582584
23andMe allrs6582584
SNP Nexus

SNPshotrs6582584
SNPdbers6582584
MSV3drs6582584
GWAS Ctlgrs6582584
GMAF0.03444
Max Magnitude0
? (C;C) (C;G) (G;G) 28
Venter snp
Source plos
Gene AG10B_HUMAN
allele G
frequency 1
sift TOLERATED
HuRef 1103649417773
Disease Association Defects in ALG10B may reduce susceptibility to acquired long QT syndrome (aLQTS) (MIM:152427). It is a cardiac anomaly characterized by a paradoxical life-threatening cardiac rhythm disturbance.



GET Evidence
ALG10B-A84G
aa_change Ala84Gly
aa_change_short A84G
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.964492
summary