rs777518512
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs777518512(C;T) |
Make rs777518512(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 39665864 |
Gene | TCAP |
is a | snp |
is | mentioned by |
dbSNP | rs777518512 |
dbSNP (classic) | rs777518512 |
ClinGen | rs777518512 |
ebi | rs777518512 |
HLI | rs777518512 |
Exac | rs777518512 |
Gnomad | rs777518512 |
Varsome | rs777518512 |
LitVar | rs777518512 |
Map | rs777518512 |
PheGenI | rs777518512 |
Biobank | rs777518512 |
1000 genomes | rs777518512 |
hgdp | rs777518512 |
ensembl | rs777518512 |
geneview | rs777518512 |
scholar | rs777518512 |
rs777518512 | |
pharmgkb | rs777518512 |
gwascentral | rs777518512 |
openSNP | rs777518512 |
23andMe | rs777518512 |
SNPshot | rs777518512 |
SNPdbe | rs777518512 |
MSV3d | rs777518512 |
GWAS Ctlg | rs777518512 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs777518512(T;T) |
Alt | rs777518512(T;T) |
Reference | Rs777518512(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TCAP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.37822117C>T |
CLNSRC | |
CLNACC | RCV000183919.2, |