rs879254112
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs879254112(A;G) |
Make rs879254112(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 14 |
Position | 102002823 |
Gene | DYNC1H1 |
is a | snp |
is | mentioned by |
dbSNP | rs879254112 |
dbSNP (classic) | rs879254112 |
ClinGen | rs879254112 |
ebi | rs879254112 |
HLI | rs879254112 |
Exac | rs879254112 |
Gnomad | rs879254112 |
Varsome | rs879254112 |
LitVar | rs879254112 |
Map | rs879254112 |
PheGenI | rs879254112 |
Biobank | rs879254112 |
1000 genomes | rs879254112 |
hgdp | rs879254112 |
ensembl | rs879254112 |
geneview | rs879254112 |
scholar | rs879254112 |
rs879254112 | |
pharmgkb | rs879254112 |
gwascentral | rs879254112 |
openSNP | rs879254112 |
23andMe | rs879254112 |
SNPshot | rs879254112 |
SNPdbe | rs879254112 |
MSV3d | rs879254112 |
GWAS Ctlg | rs879254112 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879254112(G;G) |
Alt | rs879254112(G;G) |
Reference | Rs879254112(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYNC1H1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.102469160A>G |
CLNSRC | |
CLNACC | RCV000236919.1, |