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rs1057520911

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520911(A;A)
Make rs1057520911(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position6592444
GeneCHD4
is asnp
is mentioned by
dbSNPrs1057520911
dbSNP (old)rs1057520911
ClinGenrs1057520911
ebirs1057520911
HLIrs1057520911
Exacrs1057520911
Gnomadrs1057520911
Varsomers1057520911
Maprs1057520911
PheGenIrs1057520911
Biobankrs1057520911
1000 genomesrs1057520911
hgdprs1057520911
ensemblrs1057520911
gopubmedrs1057520911
geneviewrs1057520911
scholarrs1057520911
googlers1057520911
pharmgkbrs1057520911
gwascentralrs1057520911
openSNPrs1057520911
23andMers1057520911
23andMe allrs1057520911
SNPshotrs1057520911
SNPdbers1057520911
MSV3drs1057520911
GWAS Ctlgrs1057520911
Max Magnitude0
ClinVar
Risk rs1057520911(A;A)
Alt rs1057520911(A;A)
Reference Rs1057520911(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD4
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.6701610A>T
CLNSRC
CLNACC RCV000419342.1,