rs61732609
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs61732609(C;C) |
Make rs61732609(C;T) |
Make rs61732609(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 42627674 |
Gene | CYB5R3 |
is a | snp |
is | mentioned by |
dbSNP | rs61732609 |
dbSNP (classic) | rs61732609 |
ClinGen | rs61732609 |
ebi | rs61732609 |
HLI | rs61732609 |
Exac | rs61732609 |
Gnomad | rs61732609 |
Varsome | rs61732609 |
LitVar | rs61732609 |
Map | rs61732609 |
PheGenI | rs61732609 |
Biobank | rs61732609 |
1000 genomes | rs61732609 |
hgdp | rs61732609 |
ensembl | rs61732609 |
geneview | rs61732609 |
scholar | rs61732609 |
rs61732609 | |
pharmgkb | rs61732609 |
gwascentral | rs61732609 |
openSNP | rs61732609 |
23andMe | rs61732609 |
SNPshot | rs61732609 |
SNPdbe | rs61732609 |
MSV3d | rs61732609 |
GWAS Ctlg | rs61732609 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61732609(A;A) |
Alt | rs61732609(A;A) |
Reference | Rs61732609(G;G) |
Significance | Pathogenic |
Disease | Methemoglobinemia type 2 |
Variation | info |
Gene | CYB5R3 |
CLNDBN | Methemoglobinemia type 2 |
Reversed | 0 |
HGVS | NC_000022.10:g.43023680G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000272.3, |