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rs1057518332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518332(C;T)
Make rs1057518332(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position106230366
GeneTBCK
is asnp
is mentioned by
dbSNPrs1057518332
dbSNP (old)rs1057518332
ClinGenrs1057518332
ebirs1057518332
HLIrs1057518332
Exacrs1057518332
Gnomadrs1057518332
Varsomers1057518332
Maprs1057518332
PheGenIrs1057518332
Biobankrs1057518332
1000 genomesrs1057518332
hgdprs1057518332
ensemblrs1057518332
gopubmedrs1057518332
geneviewrs1057518332
scholarrs1057518332
googlers1057518332
pharmgkbrs1057518332
gwascentralrs1057518332
openSNPrs1057518332
23andMers1057518332
23andMe allrs1057518332
SNPshotrs1057518332
SNPdbers1057518332
MSV3drs1057518332
GWAS Ctlgrs1057518332
Max Magnitude0
ClinVar
Risk rs1057518332(T;T)
Alt rs1057518332(T;T)
Reference Rs1057518332(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TBCK
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.107151523G>A
CLNSRC
CLNACC RCV000413719.1,