rs878852996
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878852996(A;A) |
Make rs878852996(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 103316544 |
Gene | DYNC2H1 |
is a | snp |
is | mentioned by |
dbSNP | rs878852996 |
dbSNP (classic) | rs878852996 |
ClinGen | rs878852996 |
ebi | rs878852996 |
HLI | rs878852996 |
Exac | rs878852996 |
Gnomad | rs878852996 |
Varsome | rs878852996 |
LitVar | rs878852996 |
Map | rs878852996 |
PheGenI | rs878852996 |
Biobank | rs878852996 |
1000 genomes | rs878852996 |
hgdp | rs878852996 |
ensembl | rs878852996 |
geneview | rs878852996 |
scholar | rs878852996 |
rs878852996 | |
pharmgkb | rs878852996 |
gwascentral | rs878852996 |
openSNP | rs878852996 |
23andMe | rs878852996 |
SNPshot | rs878852996 |
SNPdbe | rs878852996 |
MSV3d | rs878852996 |
GWAS Ctlg | rs878852996 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878852996(A;A) |
Alt | rs878852996(A;A) |
Reference | Rs878852996(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYNC2H1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.103187273G>A |
CLNSRC | |
CLNACC | RCV000224567.1, |