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rs6013382

From SNPedia

Orientationplus
Stabilizedplus
Make rs6013382(C;C)
Make rs6013382(C;T)
Make rs6013382(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position52086094
GeneZFP64
is asnp
is mentioned by
dbSNPrs6013382
ebirs6013382
HLIrs6013382
Exacrs6013382
Varsomers6013382
Maprs6013382
PheGenIrs6013382
hapmaprs6013382
1000 genomesrs6013382
hgdprs6013382
ensemblrs6013382
gopubmedrs6013382
geneviewrs6013382
scholarrs6013382
googlers6013382
pharmgkbrs6013382
gwascentralrs6013382
openSNPrs6013382
23andMers6013382
23andMe allrs6013382
SNP Nexus

SNPshotrs6013382
SNPdbers6013382
MSV3drs6013382
GWAS Ctlgrs6013382
GMAF0.4536
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs6013382
PubMedID [PMID 17362836]
Condition Amyotrophic lateral sclerosis
Gene ZFP64
Risk Allele
pValue 5.00E-006
OR 1.43
95% CI 1.11-1.67



GET Evidence
rs6013382
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.483871
summary