rs770045008
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs770045008(C;T) |
Make rs770045008(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 35503626 |
Gene | TULP1 |
is a | snp |
is | mentioned by |
dbSNP | rs770045008 |
dbSNP (classic) | rs770045008 |
ClinGen | rs770045008 |
ebi | rs770045008 |
HLI | rs770045008 |
Exac | rs770045008 |
Gnomad | rs770045008 |
Varsome | rs770045008 |
LitVar | rs770045008 |
Map | rs770045008 |
PheGenI | rs770045008 |
Biobank | rs770045008 |
1000 genomes | rs770045008 |
hgdp | rs770045008 |
ensembl | rs770045008 |
geneview | rs770045008 |
scholar | rs770045008 |
rs770045008 | |
pharmgkb | rs770045008 |
gwascentral | rs770045008 |
openSNP | rs770045008 |
23andMe | rs770045008 |
SNPshot | rs770045008 |
SNPdbe | rs770045008 |
MSV3d | rs770045008 |
GWAS Ctlg | rs770045008 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770045008(T;T) |
Alt | rs770045008(T;T) |
Reference | Rs770045008(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TULP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.35471403C>T |
CLNSRC | |
CLNACC | RCV000171394.1, |