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rs1057517932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517932(A;C)
Make rs1057517932(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position3227489
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs1057517932
dbSNP (old)rs1057517932
ClinGenrs1057517932
ebirs1057517932
HLIrs1057517932
Exacrs1057517932
Gnomadrs1057517932
Varsomers1057517932
LitVarrs1057517932
Maprs1057517932
PheGenIrs1057517932
Biobankrs1057517932
1000 genomesrs1057517932
hgdprs1057517932
ensemblrs1057517932
gopubmedrs1057517932
geneviewrs1057517932
scholarrs1057517932
googlers1057517932
pharmgkbrs1057517932
gwascentralrs1057517932
openSNPrs1057517932
23andMers1057517932
23andMe allrs1057517932
SNPshotrs1057517932
SNPdbers1057517932
MSV3drs1057517932
GWAS Ctlgrs1057517932
Max Magnitude0
ClinVar
Risk rs1057517932(C;C)
Alt rs1057517932(C;C)
Reference Rs1057517932(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TUBB2B
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.3227723T>G
CLNSRC
CLNACC RCV000414164.1,