rs780085174
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs780085174(C;T) |
Make rs780085174(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 53102097 |
Gene | MOCS2 |
is a | snp |
is | mentioned by |
dbSNP | rs780085174 |
dbSNP (classic) | rs780085174 |
ClinGen | rs780085174 |
ebi | rs780085174 |
HLI | rs780085174 |
Exac | rs780085174 |
Gnomad | rs780085174 |
Varsome | rs780085174 |
LitVar | rs780085174 |
Map | rs780085174 |
PheGenI | rs780085174 |
Biobank | rs780085174 |
1000 genomes | rs780085174 |
hgdp | rs780085174 |
ensembl | rs780085174 |
geneview | rs780085174 |
scholar | rs780085174 |
rs780085174 | |
pharmgkb | rs780085174 |
gwascentral | rs780085174 |
openSNP | rs780085174 |
23andMe | rs780085174 |
SNPshot | rs780085174 |
SNPdbe | rs780085174 |
MSV3d | rs780085174 |
GWAS Ctlg | rs780085174 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs780085174(T;T) |
Alt | rs780085174(T;T) |
Reference | Rs780085174(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MOCS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.52397927C>T |
CLNSRC | |
CLNACC | RCV000479116.1, |