rs755299132
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs755299132(C;T) |
Make rs755299132(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 91220906 |
Gene | AUH |
is a | snp |
is | mentioned by |
dbSNP | rs755299132 |
dbSNP (classic) | rs755299132 |
ClinGen | rs755299132 |
ebi | rs755299132 |
HLI | rs755299132 |
Exac | rs755299132 |
Gnomad | rs755299132 |
Varsome | rs755299132 |
LitVar | rs755299132 |
Map | rs755299132 |
PheGenI | rs755299132 |
Biobank | rs755299132 |
1000 genomes | rs755299132 |
hgdp | rs755299132 |
ensembl | rs755299132 |
geneview | rs755299132 |
scholar | rs755299132 |
rs755299132 | |
pharmgkb | rs755299132 |
gwascentral | rs755299132 |
openSNP | rs755299132 |
23andMe | rs755299132 |
SNPshot | rs755299132 |
SNPdbe | rs755299132 |
MSV3d | rs755299132 |
GWAS Ctlg | rs755299132 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755299132(T;T) |
Alt | rs755299132(T;T) |
Reference | Rs755299132(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | AUH |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.93983188C>T |
CLNSRC | |
CLNACC | RCV000197560.1, |