rs34071856
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs34071856(G;G) |
Make rs34071856(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177075 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs34071856 |
dbSNP (classic) | rs34071856 |
ClinGen | rs34071856 |
ebi | rs34071856 |
HLI | rs34071856 |
Exac | rs34071856 |
Gnomad | rs34071856 |
Varsome | rs34071856 |
LitVar | rs34071856 |
Map | rs34071856 |
PheGenI | rs34071856 |
Biobank | rs34071856 |
1000 genomes | rs34071856 |
hgdp | rs34071856 |
ensembl | rs34071856 |
geneview | rs34071856 |
scholar | rs34071856 |
rs34071856 | |
pharmgkb | rs34071856 |
gwascentral | rs34071856 |
openSNP | rs34071856 |
23andMe | rs34071856 |
SNPshot | rs34071856 |
SNPdbe | rs34071856 |
MSV3d | rs34071856 |
GWAS Ctlg | rs34071856 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34071856(G;G) |
Alt | rs34071856(G;G) |
Reference | Rs34071856(T;T) |
Significance | Other |
Disease | HEMOGLOBIN ANN ARBOR |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN ANN ARBOR |
Reversed | 0 |
HGVS | NC_000016.9:g.227074T>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000016990.2, |
[PMID 5033650] Biosynthesis of hemoglobin Ann Arbor: evidence for catabolic and feedback regulation.