rs879253971
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs879253971(G;T) |
Make rs879253971(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 14 |
Position | 102016944 |
Gene | DYNC1H1 |
is a | snp |
is | mentioned by |
dbSNP | rs879253971 |
dbSNP (classic) | rs879253971 |
ClinGen | rs879253971 |
ebi | rs879253971 |
HLI | rs879253971 |
Exac | rs879253971 |
Gnomad | rs879253971 |
Varsome | rs879253971 |
LitVar | rs879253971 |
Map | rs879253971 |
PheGenI | rs879253971 |
Biobank | rs879253971 |
1000 genomes | rs879253971 |
hgdp | rs879253971 |
ensembl | rs879253971 |
geneview | rs879253971 |
scholar | rs879253971 |
rs879253971 | |
pharmgkb | rs879253971 |
gwascentral | rs879253971 |
openSNP | rs879253971 |
23andMe | rs879253971 |
SNPshot | rs879253971 |
SNPdbe | rs879253971 |
MSV3d | rs879253971 |
GWAS Ctlg | rs879253971 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879253971(T;T) |
Alt | rs879253971(T;T) |
Reference | Rs879253971(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYNC1H1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.102483281G>T |
CLNSRC | |
CLNACC | RCV000235681.1, |