rs746386175
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs746386175(G;T) |
Make rs746386175(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 121162074 |
Gene | TECTA |
is a | snp |
is | mentioned by |
dbSNP | rs746386175 |
dbSNP (classic) | rs746386175 |
ClinGen | rs746386175 |
ebi | rs746386175 |
HLI | rs746386175 |
Exac | rs746386175 |
Gnomad | rs746386175 |
Varsome | rs746386175 |
LitVar | rs746386175 |
Map | rs746386175 |
PheGenI | rs746386175 |
Biobank | rs746386175 |
1000 genomes | rs746386175 |
hgdp | rs746386175 |
ensembl | rs746386175 |
geneview | rs746386175 |
scholar | rs746386175 |
rs746386175 | |
pharmgkb | rs746386175 |
gwascentral | rs746386175 |
openSNP | rs746386175 |
23andMe | rs746386175 |
SNPshot | rs746386175 |
SNPdbe | rs746386175 |
MSV3d | rs746386175 |
GWAS Ctlg | rs746386175 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs746386175(T;T) |
Alt | rs746386175(T;T) |
Reference | Rs746386175(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TECTA |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.121032783G>T |
CLNSRC | |
CLNACC | RCV000485051.1, |