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rs1057517934

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517934(C;T)
Make rs1057517934(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position149378318
GeneTAB2
is asnp
is mentioned by
dbSNPrs1057517934
dbSNP (old)rs1057517934
ClinGenrs1057517934
ebirs1057517934
HLIrs1057517934
Exacrs1057517934
Gnomadrs1057517934
Varsomers1057517934
Maprs1057517934
PheGenIrs1057517934
Biobankrs1057517934
1000 genomesrs1057517934
hgdprs1057517934
ensemblrs1057517934
gopubmedrs1057517934
geneviewrs1057517934
scholarrs1057517934
googlers1057517934
pharmgkbrs1057517934
gwascentralrs1057517934
openSNPrs1057517934
23andMers1057517934
23andMe allrs1057517934
SNPshotrs1057517934
SNPdbers1057517934
MSV3drs1057517934
GWAS Ctlgrs1057517934
Max Magnitude0
ClinVar
Risk rs1057517934(T;T)
Alt rs1057517934(T;T)
Reference Rs1057517934(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TAB2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.149699454C>T
CLNSRC
CLNACC RCV000413501.1,