rs41364652
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs41364652(A;A) |
Make rs41364652(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 173580 |
Gene | HBA2 |
is a | snp |
is | mentioned by |
dbSNP | rs41364652 |
dbSNP (classic) | rs41364652 |
ClinGen | rs41364652 |
ebi | rs41364652 |
HLI | rs41364652 |
Exac | rs41364652 |
Gnomad | rs41364652 |
Varsome | rs41364652 |
LitVar | rs41364652 |
Map | rs41364652 |
PheGenI | rs41364652 |
Biobank | rs41364652 |
1000 genomes | rs41364652 |
hgdp | rs41364652 |
ensembl | rs41364652 |
geneview | rs41364652 |
scholar | rs41364652 |
rs41364652 | |
pharmgkb | rs41364652 |
gwascentral | rs41364652 |
openSNP | rs41364652 |
23andMe | rs41364652 |
SNPshot | rs41364652 |
SNPdbe | rs41364652 |
MSV3d | rs41364652 |
GWAS Ctlg | rs41364652 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41364652(A;A) |
Alt | rs41364652(A;A) |
Reference | Rs41364652(C;C) |
Significance | Untested |
Disease | |
Variation | info |
Gene | HBA2 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000016.9:g.223579C>A |
CLNSRC | |
CLNACC |
[PMID 3781866] HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black family.
[PMID 7803274] The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.
[PMID 8226092] Three sickle cell anemia patients each with a different alpha chain variant. Diagnostic complications.