rs935526225
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs935526225(A;A) |
Make rs935526225(A;G) |
Make rs935526225(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 6616521 |
Gene | TPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs935526225 |
dbSNP (classic) | rs935526225 |
ClinGen | rs935526225 |
ebi | rs935526225 |
HLI | rs935526225 |
Exac | rs935526225 |
Gnomad | rs935526225 |
Varsome | rs935526225 |
LitVar | rs935526225 |
Map | rs935526225 |
PheGenI | rs935526225 |
Biobank | rs935526225 |
1000 genomes | rs935526225 |
hgdp | rs935526225 |
ensembl | rs935526225 |
geneview | rs935526225 |
scholar | rs935526225 |
rs935526225 | |
pharmgkb | rs935526225 |
gwascentral | rs935526225 |
openSNP | rs935526225 |
23andMe | rs935526225 |
SNPshot | rs935526225 |
SNPdbe | rs935526225 |
MSV3d | rs935526225 |
GWAS Ctlg | rs935526225 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs935526225(C;C) |
Alt | rs935526225(C;C) |
Reference | Rs935526225(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TPP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.6637752T>C |
CLNSRC | |
CLNACC | RCV000428562.1, |