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rs1057517996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517996(C;C)
Make rs1057517996(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position59024206
GeneTUBB1
is asnp
is mentioned by
dbSNPrs1057517996
dbSNP (old)rs1057517996
ClinGenrs1057517996
ebirs1057517996
HLIrs1057517996
Exacrs1057517996
Gnomadrs1057517996
Varsomers1057517996
LitVarrs1057517996
Maprs1057517996
PheGenIrs1057517996
Biobankrs1057517996
1000 genomesrs1057517996
hgdprs1057517996
ensemblrs1057517996
gopubmedrs1057517996
geneviewrs1057517996
scholarrs1057517996
googlers1057517996
pharmgkbrs1057517996
gwascentralrs1057517996
openSNPrs1057517996
23andMers1057517996
23andMe allrs1057517996
SNPshotrs1057517996
SNPdbers1057517996
MSV3drs1057517996
GWAS Ctlgrs1057517996
Max Magnitude0
ClinVar
Risk rs1057517996(C;C)
Alt rs1057517996(C;C)
Reference Rs1057517996(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TUBB1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.57599261T>C
CLNSRC
CLNACC RCV000413950.1,