Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520391(C;T)
Make rs1057520391(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position3225556
GeneTUBB2B
is asnp
is mentioned by
dbSNPrs1057520391
dbSNP (old)rs1057520391
ClinGenrs1057520391
ebirs1057520391
HLIrs1057520391
Exacrs1057520391
Gnomadrs1057520391
Varsomers1057520391
Maprs1057520391
PheGenIrs1057520391
Biobankrs1057520391
1000 genomesrs1057520391
hgdprs1057520391
ensemblrs1057520391
gopubmedrs1057520391
geneviewrs1057520391
scholarrs1057520391
googlers1057520391
pharmgkbrs1057520391
gwascentralrs1057520391
openSNPrs1057520391
23andMers1057520391
23andMe allrs1057520391
SNPshotrs1057520391
SNPdbers1057520391
MSV3drs1057520391
GWAS Ctlgrs1057520391
Max Magnitude0
ClinVar
Risk rs1057520391(T;T)
Alt rs1057520391(T;T)
Reference Rs1057520391(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TUBB2B
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.3225790G>A
CLNSRC
CLNACC RCV000421828.1,