rs33922873
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs33922873(C;T) |
Make rs33922873(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5226702 |
Gene | HBB |
is a | snp |
is | mentioned by |
dbSNP | rs33922873 |
dbSNP (classic) | rs33922873 |
ClinGen | rs33922873 |
ebi | rs33922873 |
HLI | rs33922873 |
Exac | rs33922873 |
Gnomad | rs33922873 |
Varsome | rs33922873 |
LitVar | rs33922873 |
Map | rs33922873 |
PheGenI | rs33922873 |
Biobank | rs33922873 |
1000 genomes | rs33922873 |
hgdp | rs33922873 |
ensembl | rs33922873 |
geneview | rs33922873 |
scholar | rs33922873 |
rs33922873 | |
pharmgkb | rs33922873 |
gwascentral | rs33922873 |
openSNP | rs33922873 |
23andMe | rs33922873 |
SNPshot | rs33922873 |
SNPdbe | rs33922873 |
MSV3d | rs33922873 |
GWAS Ctlg | rs33922873 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs33922873(A;A) rs33922873(T;T) |
Alt | rs33922873(A;A) rs33922873(T;T) |
Reference | Rs33922873(C;C) |
Significance | Other |
Disease | HEMOGLOBIN M (SASKATOON) |
Variation | info |
Gene | HBB |
CLNDBN | HEMOGLOBIN M (SASKATOON) |
Reversed | 1 |
HGVS | NC_000011.9:g.5247932G>A |
CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000016466.5, |
[PMID 9601847] [Hemoglobin Hana or alpha 2 beta 2 63 (E7) His-Asn: a new unstable hemoglobin variant with a paradoxically different clinical manifestations in smokers and non-smokers in the same family].