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rs1057518015

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518015(C;T)
Make rs1057518015(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position149379110
GeneTAB2
is asnp
is mentioned by
dbSNPrs1057518015
dbSNP (old)rs1057518015
ClinGenrs1057518015
ebirs1057518015
HLIrs1057518015
Exacrs1057518015
Gnomadrs1057518015
Varsomers1057518015
Maprs1057518015
PheGenIrs1057518015
Biobankrs1057518015
1000 genomesrs1057518015
hgdprs1057518015
ensemblrs1057518015
gopubmedrs1057518015
geneviewrs1057518015
scholarrs1057518015
googlers1057518015
pharmgkbrs1057518015
gwascentralrs1057518015
openSNPrs1057518015
23andMers1057518015
23andMe allrs1057518015
SNPshotrs1057518015
SNPdbers1057518015
MSV3drs1057518015
GWAS Ctlgrs1057518015
Max Magnitude0
ClinVar
Risk rs1057518015(T;T)
Alt rs1057518015(T;T)
Reference Rs1057518015(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TAB2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.149700246C>T
CLNSRC
CLNACC RCV000414624.1,