rs761622153
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs761622153(A;A) |
Make rs761622153(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 13841112 |
Gene | DNAH5 |
is a | snp |
is | mentioned by |
dbSNP | rs761622153 |
dbSNP (classic) | rs761622153 |
ClinGen | rs761622153 |
ebi | rs761622153 |
HLI | rs761622153 |
Exac | rs761622153 |
Gnomad | rs761622153 |
Varsome | rs761622153 |
LitVar | rs761622153 |
Map | rs761622153 |
PheGenI | rs761622153 |
Biobank | rs761622153 |
1000 genomes | rs761622153 |
hgdp | rs761622153 |
ensembl | rs761622153 |
geneview | rs761622153 |
scholar | rs761622153 |
rs761622153 | |
pharmgkb | rs761622153 |
gwascentral | rs761622153 |
openSNP | rs761622153 |
23andMe | rs761622153 |
SNPshot | rs761622153 |
SNPdbe | rs761622153 |
MSV3d | rs761622153 |
GWAS Ctlg | rs761622153 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761622153(A;A) |
Alt | rs761622153(A;A) |
Reference | Rs761622153(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNAH5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.13841221G>A |
CLNSRC | |
CLNACC | RCV000413667.1, |