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rs1057517699

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517699(A;A)
Make rs1057517699(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position64328511
GeneTECRL
is asnp
is mentioned by
dbSNPrs1057517699
dbSNP (old)rs1057517699
ClinGenrs1057517699
ebirs1057517699
HLIrs1057517699
Exacrs1057517699
Gnomadrs1057517699
Varsomers1057517699
Maprs1057517699
PheGenIrs1057517699
Biobankrs1057517699
1000 genomesrs1057517699
hgdprs1057517699
ensemblrs1057517699
gopubmedrs1057517699
geneviewrs1057517699
scholarrs1057517699
googlers1057517699
pharmgkbrs1057517699
gwascentralrs1057517699
openSNPrs1057517699
23andMers1057517699
23andMe allrs1057517699
SNPshotrs1057517699
SNPdbers1057517699
MSV3drs1057517699
GWAS Ctlgrs1057517699
Max Magnitude0
ClinVar
Risk rs1057517699(A;A)
Alt rs1057517699(A;A)
Reference Rs1057517699(G;G)
Significance Pathogenic
Disease Ventricular tachycardia
Variation info
Gene TECRL
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 3
Reversed 1
HGVS NC_000004.11:g.65194229C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000412582.1,