rs777854951
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs777854951(G;T) |
Make rs777854951(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 21741710 |
Gene | MIB1 |
is a | snp |
is | mentioned by |
dbSNP | rs777854951 |
dbSNP (classic) | rs777854951 |
ClinGen | rs777854951 |
ebi | rs777854951 |
HLI | rs777854951 |
Exac | rs777854951 |
Gnomad | rs777854951 |
Varsome | rs777854951 |
LitVar | rs777854951 |
Map | rs777854951 |
PheGenI | rs777854951 |
Biobank | rs777854951 |
1000 genomes | rs777854951 |
hgdp | rs777854951 |
ensembl | rs777854951 |
geneview | rs777854951 |
scholar | rs777854951 |
rs777854951 | |
pharmgkb | rs777854951 |
gwascentral | rs777854951 |
openSNP | rs777854951 |
23andMe | rs777854951 |
SNPshot | rs777854951 |
SNPdbe | rs777854951 |
MSV3d | rs777854951 |
GWAS Ctlg | rs777854951 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs777854951(T;T) |
Alt | rs777854951(T;T) |
Reference | Rs777854951(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MIB1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.19321671G>T |
CLNSRC | |
CLNACC | RCV000432654.1, |