rs878853284
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878853284(G;T) |
Make rs878853284(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 3225373 |
Gene | TUBB2B |
is a | snp |
is | mentioned by |
dbSNP | rs878853284 |
dbSNP (classic) | rs878853284 |
ClinGen | rs878853284 |
ebi | rs878853284 |
HLI | rs878853284 |
Exac | rs878853284 |
Gnomad | rs878853284 |
Varsome | rs878853284 |
LitVar | rs878853284 |
Map | rs878853284 |
PheGenI | rs878853284 |
Biobank | rs878853284 |
1000 genomes | rs878853284 |
hgdp | rs878853284 |
ensembl | rs878853284 |
geneview | rs878853284 |
scholar | rs878853284 |
rs878853284 | |
pharmgkb | rs878853284 |
gwascentral | rs878853284 |
openSNP | rs878853284 |
23andMe | rs878853284 |
SNPshot | rs878853284 |
SNPdbe | rs878853284 |
MSV3d | rs878853284 |
GWAS Ctlg | rs878853284 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853284(T;T) |
Alt | rs878853284(T;T) |
Reference | Rs878853284(G;G) |
Significance | Pathogenic |
Disease | Polymicrogyria |
Variation | info |
Gene | TUBB2B |
CLNDBN | Polymicrogyria, asymmetric |
Reversed | 1 |
HGVS | NC_000006.11:g.3225607C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000225257.1, |