rs35166834
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs35166834(G;G) |
Make rs35166834(G;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 177380 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs35166834 |
dbSNP (classic) | rs35166834 |
ClinGen | rs35166834 |
ebi | rs35166834 |
HLI | rs35166834 |
Exac | rs35166834 |
Gnomad | rs35166834 |
Varsome | rs35166834 |
LitVar | rs35166834 |
Map | rs35166834 |
PheGenI | rs35166834 |
Biobank | rs35166834 |
1000 genomes | rs35166834 |
hgdp | rs35166834 |
ensembl | rs35166834 |
geneview | rs35166834 |
scholar | rs35166834 |
rs35166834 | |
pharmgkb | rs35166834 |
gwascentral | rs35166834 |
openSNP | rs35166834 |
23andMe | rs35166834 |
SNPshot | rs35166834 |
SNPdbe | rs35166834 |
MSV3d | rs35166834 |
GWAS Ctlg | rs35166834 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35166834(G;G) |
Alt | rs35166834(G;G) |
Reference | Rs35166834(T;T) |
Significance | Other |
Disease | HEMOGLOBIN CAEN |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN CAEN |
Reversed | 0 |
HGVS | NC_000016.9:g.227379T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000017197.2, |
[PMID 8493987] Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly).