rs746085696
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs746085696(C;T) |
Make rs746085696(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 6619191 |
Gene | TPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs746085696 |
dbSNP (classic) | rs746085696 |
ClinGen | rs746085696 |
ebi | rs746085696 |
HLI | rs746085696 |
Exac | rs746085696 |
Gnomad | rs746085696 |
Varsome | rs746085696 |
LitVar | rs746085696 |
Map | rs746085696 |
PheGenI | rs746085696 |
Biobank | rs746085696 |
1000 genomes | rs746085696 |
hgdp | rs746085696 |
ensembl | rs746085696 |
geneview | rs746085696 |
scholar | rs746085696 |
rs746085696 | |
pharmgkb | rs746085696 |
gwascentral | rs746085696 |
openSNP | rs746085696 |
23andMe | rs746085696 |
SNPshot | rs746085696 |
SNPdbe | rs746085696 |
MSV3d | rs746085696 |
GWAS Ctlg | rs746085696 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs746085696(G;G) rs746085696(T;T) |
Alt | rs746085696(G;G) rs746085696(T;T) |
Reference | Rs746085696(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TPP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.6640422C>G |
CLNSRC | |
CLNACC | RCV000189799.1, |