rs35859529
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs35859529(A;G) |
Make rs35859529(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177051 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs35859529 |
dbSNP (classic) | rs35859529 |
ClinGen | rs35859529 |
ebi | rs35859529 |
HLI | rs35859529 |
Exac | rs35859529 |
Gnomad | rs35859529 |
Varsome | rs35859529 |
LitVar | rs35859529 |
Map | rs35859529 |
PheGenI | rs35859529 |
Biobank | rs35859529 |
1000 genomes | rs35859529 |
hgdp | rs35859529 |
ensembl | rs35859529 |
geneview | rs35859529 |
scholar | rs35859529 |
rs35859529 | |
pharmgkb | rs35859529 |
gwascentral | rs35859529 |
openSNP | rs35859529 |
23andMe | rs35859529 |
SNPshot | rs35859529 |
SNPdbe | rs35859529 |
MSV3d | rs35859529 |
GWAS Ctlg | rs35859529 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35859529(G;G) |
Alt | rs35859529(G;G) |
Reference | Rs35859529(A;A) |
Significance | Other |
Disease | HEMOGLOBIN DANESHGAH-TEHRAN |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN DANESHGAH-TEHRAN |
Reversed | 0 |
HGVS | NC_000016.9:g.227050A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017013.2, |
[PMID 3841101] Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family.
[PMID 4518991] Haemoglobin Daneshgah-Tehran alpha2 72 (EPI) histidine--arginine betaA2.