rs879254267
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs879254267(A;T) |
Make rs879254267(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 14 |
Position | 101983070 |
Gene | DYNC1H1 |
is a | snp |
is | mentioned by |
dbSNP | rs879254267 |
dbSNP (classic) | rs879254267 |
ClinGen | rs879254267 |
ebi | rs879254267 |
HLI | rs879254267 |
Exac | rs879254267 |
Gnomad | rs879254267 |
Varsome | rs879254267 |
LitVar | rs879254267 |
Map | rs879254267 |
PheGenI | rs879254267 |
Biobank | rs879254267 |
1000 genomes | rs879254267 |
hgdp | rs879254267 |
ensembl | rs879254267 |
geneview | rs879254267 |
scholar | rs879254267 |
rs879254267 | |
pharmgkb | rs879254267 |
gwascentral | rs879254267 |
openSNP | rs879254267 |
23andMe | rs879254267 |
SNPshot | rs879254267 |
SNPdbe | rs879254267 |
MSV3d | rs879254267 |
GWAS Ctlg | rs879254267 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879254267(T;T) |
Alt | rs879254267(T;T) |
Reference | Rs879254267(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYNC1H1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.102449407A>T |
CLNSRC | |
CLNACC | RCV000236737.1, |