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rs1057518437

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518437(A;A)
Make rs1057518437(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position149378166
GeneTAB2
is asnp
is mentioned by
dbSNPrs1057518437
dbSNP (old)rs1057518437
ClinGenrs1057518437
ebirs1057518437
HLIrs1057518437
Exacrs1057518437
Gnomadrs1057518437
Varsomers1057518437
Maprs1057518437
PheGenIrs1057518437
Biobankrs1057518437
1000 genomesrs1057518437
hgdprs1057518437
ensemblrs1057518437
gopubmedrs1057518437
geneviewrs1057518437
scholarrs1057518437
googlers1057518437
pharmgkbrs1057518437
gwascentralrs1057518437
openSNPrs1057518437
23andMers1057518437
23andMe allrs1057518437
SNPshotrs1057518437
SNPdbers1057518437
MSV3drs1057518437
GWAS Ctlgrs1057518437
Max Magnitude0
ClinVar
Risk rs1057518437(A;A)
Alt rs1057518437(A;A)
Reference Rs1057518437(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TAB2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.149699302C>A
CLNSRC
CLNACC RCV000413051.1,