rs111033602
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs111033602(A;C) |
Make rs111033602(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 173264 |
Gene | HBA2 |
is a | snp |
is | mentioned by |
dbSNP | rs111033602 |
dbSNP (classic) | rs111033602 |
ClinGen | rs111033602 |
ebi | rs111033602 |
HLI | rs111033602 |
Exac | rs111033602 |
Gnomad | rs111033602 |
Varsome | rs111033602 |
LitVar | rs111033602 |
Map | rs111033602 |
PheGenI | rs111033602 |
Biobank | rs111033602 |
1000 genomes | rs111033602 |
hgdp | rs111033602 |
ensembl | rs111033602 |
geneview | rs111033602 |
scholar | rs111033602 |
rs111033602 | |
pharmgkb | rs111033602 |
gwascentral | rs111033602 |
openSNP | rs111033602 |
23andMe | rs111033602 |
SNPshot | rs111033602 |
SNPdbe | rs111033602 |
MSV3d | rs111033602 |
GWAS Ctlg | rs111033602 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs111033602(C;C) rs111033602(G;G) |
Alt | rs111033602(C;C) rs111033602(G;G) |
Reference | Rs111033602(A;A) |
Significance | Other |
Disease | HEMOGLOBIN DAVENPORT |
Variation | info |
Gene | HBA2 |
CLNDBN | HEMOGLOBIN DAVENPORT |
Reversed | 0 |
HGVS | NC_000016.9:g.223263A>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000016928.1, |
[PMID 6691995] Hb J-Singa (alpha-78 Asn leads to Asp), a newly discovered hemoglobin variant with the same amino acid substitution as one of the two present in Hb J-Singapore (alpha-78 Asn leads to, alpha-79 Ala leads to Gly).