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rs1057520787

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520787(C;C)
Make rs1057520787(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position3224900
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs1057520787
dbSNP (old)rs1057520787
ClinGenrs1057520787
ebirs1057520787
HLIrs1057520787
Exacrs1057520787
Gnomadrs1057520787
Varsomers1057520787
LitVarrs1057520787
Maprs1057520787
PheGenIrs1057520787
Biobankrs1057520787
1000 genomesrs1057520787
hgdprs1057520787
ensemblrs1057520787
gopubmedrs1057520787
geneviewrs1057520787
scholarrs1057520787
googlers1057520787
pharmgkbrs1057520787
gwascentralrs1057520787
openSNPrs1057520787
23andMers1057520787
23andMe allrs1057520787
SNPshotrs1057520787
SNPdbers1057520787
MSV3drs1057520787
GWAS Ctlgrs1057520787
Max Magnitude0
ClinVar
Risk rs1057520787(C;C)
Alt rs1057520787(C;C)
Reference Rs1057520787(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TUBB2B
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.3225134A>G
CLNSRC
CLNACC RCV000418450.1,