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rs1057518968

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518968(A;G)
Make rs1057518968(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position34794065
GeneDTNA
is asnp
is mentioned by
dbSNPrs1057518968
dbSNP (old)rs1057518968
ClinGenrs1057518968
ebirs1057518968
HLIrs1057518968
Exacrs1057518968
Gnomadrs1057518968
Varsomers1057518968
Maprs1057518968
PheGenIrs1057518968
Biobankrs1057518968
1000 genomesrs1057518968
hgdprs1057518968
ensemblrs1057518968
gopubmedrs1057518968
geneviewrs1057518968
scholarrs1057518968
googlers1057518968
pharmgkbrs1057518968
gwascentralrs1057518968
openSNPrs1057518968
23andMers1057518968
23andMe allrs1057518968
SNPshotrs1057518968
SNPdbers1057518968
MSV3drs1057518968
GWAS Ctlgrs1057518968
Max Magnitude0
ClinVar
Risk rs1057518968(G;G)
Alt rs1057518968(G;G)
Reference Rs1057518968(A;A)
Significance Probable-Pathogenic
Disease Arrhythmia Noncompaction cardiomyopathy
Variation info
Gene DTNA
CLNDBN Arrhythmia Noncompaction cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.32374029A>G
CLNSRC
CLNACC RCV000415295.1,