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rs1057518422

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518422(C;T)
Make rs1057518422(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position149378954
GeneTAB2
is asnp
is mentioned by
dbSNPrs1057518422
dbSNP (old)rs1057518422
ClinGenrs1057518422
ebirs1057518422
HLIrs1057518422
Exacrs1057518422
Gnomadrs1057518422
Varsomers1057518422
LitVarrs1057518422
Maprs1057518422
PheGenIrs1057518422
Biobankrs1057518422
1000 genomesrs1057518422
hgdprs1057518422
ensemblrs1057518422
gopubmedrs1057518422
geneviewrs1057518422
scholarrs1057518422
googlers1057518422
pharmgkbrs1057518422
gwascentralrs1057518422
openSNPrs1057518422
23andMers1057518422
23andMe allrs1057518422
SNPshotrs1057518422
SNPdbers1057518422
MSV3drs1057518422
GWAS Ctlgrs1057518422
Max Magnitude0
ClinVar
Risk rs1057518422(T;T)
Alt rs1057518422(T;T)
Reference Rs1057518422(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TAB2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.149700090C>T
CLNSRC
CLNACC RCV000412798.1,