rs775225727
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs775225727(A;A) |
Make rs775225727(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 69599802 |
Gene | AUTS2 |
is a | snp |
is | mentioned by |
dbSNP | rs775225727 |
dbSNP (classic) | rs775225727 |
ClinGen | rs775225727 |
ebi | rs775225727 |
HLI | rs775225727 |
Exac | rs775225727 |
Gnomad | rs775225727 |
Varsome | rs775225727 |
LitVar | rs775225727 |
Map | rs775225727 |
PheGenI | rs775225727 |
Biobank | rs775225727 |
1000 genomes | rs775225727 |
hgdp | rs775225727 |
ensembl | rs775225727 |
geneview | rs775225727 |
scholar | rs775225727 |
rs775225727 | |
pharmgkb | rs775225727 |
gwascentral | rs775225727 |
openSNP | rs775225727 |
23andMe | rs775225727 |
SNPshot | rs775225727 |
SNPdbe | rs775225727 |
MSV3d | rs775225727 |
GWAS Ctlg | rs775225727 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775225727(A;A) rs775225727(G;G) |
Alt | rs775225727(A;A) rs775225727(G;G) |
Reference | Rs775225727(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | AUTS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.69064788C>A |
CLNSRC | |
CLNACC | RCV000440958.1, |