rs869320724
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs869320724(-;GC) |
Make rs869320724(GC;GC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 37069307 |
Gene | TMPRSS6 |
is a | snp |
is | mentioned by |
dbSNP | rs869320724 |
dbSNP (classic) | rs869320724 |
ClinGen | rs869320724 |
ebi | rs869320724 |
HLI | rs869320724 |
Exac | rs869320724 |
Gnomad | rs869320724 |
Varsome | rs869320724 |
LitVar | rs869320724 |
Map | rs869320724 |
PheGenI | rs869320724 |
Biobank | rs869320724 |
1000 genomes | rs869320724 |
hgdp | rs869320724 |
ensembl | rs869320724 |
geneview | rs869320724 |
scholar | rs869320724 |
rs869320724 | |
pharmgkb | rs869320724 |
gwascentral | rs869320724 |
openSNP | rs869320724 |
23andMe | rs869320724 |
SNPshot | rs869320724 |
SNPdbe | rs869320724 |
MSV3d | rs869320724 |
GWAS Ctlg | rs869320724 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869320724(GC;GC) |
Alt | rs869320724(GC;GC) |
Reference | Rs869320724(-;-) |
Significance | Pathogenic |
Disease | Microcytic anemia |
Variation | info |
Gene | TMPRSS6 |
CLNDBN | Microcytic anemia |
Reversed | 1 |
HGVS | NC_000022.10:g.37465348_37465349dupGC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000001464.3, |