rs575017579
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs575017579(A;A) |
Make rs575017579(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 13840968 |
Gene | DNAH5 |
is a | snp |
is | mentioned by |
dbSNP | rs575017579 |
dbSNP (classic) | rs575017579 |
ClinGen | rs575017579 |
ebi | rs575017579 |
HLI | rs575017579 |
Exac | rs575017579 |
Gnomad | rs575017579 |
Varsome | rs575017579 |
LitVar | rs575017579 |
Map | rs575017579 |
PheGenI | rs575017579 |
Biobank | rs575017579 |
1000 genomes | rs575017579 |
hgdp | rs575017579 |
ensembl | rs575017579 |
geneview | rs575017579 |
scholar | rs575017579 |
rs575017579 | |
pharmgkb | rs575017579 |
gwascentral | rs575017579 |
openSNP | rs575017579 |
23andMe | rs575017579 |
SNPshot | rs575017579 |
SNPdbe | rs575017579 |
MSV3d | rs575017579 |
GWAS Ctlg | rs575017579 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs575017579(A;A) rs575017579(C;C) |
Alt | rs575017579(A;A) rs575017579(C;C) |
Reference | Rs575017579(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNAH5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.13841077G>A |
CLNSRC | |
CLNACC | RCV000494045.1, |