rs1057517996
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1057517996(C;C) |
Make rs1057517996(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 59024206 |
Gene | TUBB1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517996 |
dbSNP (classic) | rs1057517996 |
ClinGen | rs1057517996 |
ebi | rs1057517996 |
HLI | rs1057517996 |
Exac | rs1057517996 |
Gnomad | rs1057517996 |
Varsome | rs1057517996 |
LitVar | rs1057517996 |
Map | rs1057517996 |
PheGenI | rs1057517996 |
Biobank | rs1057517996 |
1000 genomes | rs1057517996 |
hgdp | rs1057517996 |
ensembl | rs1057517996 |
geneview | rs1057517996 |
scholar | rs1057517996 |
rs1057517996 | |
pharmgkb | rs1057517996 |
gwascentral | rs1057517996 |
openSNP | rs1057517996 |
23andMe | rs1057517996 |
SNPshot | rs1057517996 |
SNPdbe | rs1057517996 |
MSV3d | rs1057517996 |
GWAS Ctlg | rs1057517996 |
Max Magnitude | 0 |
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, |