rs41338947
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs41338947(A;A) |
Make rs41338947(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 173323 |
Gene | HBA2 |
is a | snp |
is | mentioned by |
dbSNP | rs41338947 |
dbSNP (classic) | rs41338947 |
ClinGen | rs41338947 |
ebi | rs41338947 |
HLI | rs41338947 |
Exac | rs41338947 |
Gnomad | rs41338947 |
Varsome | rs41338947 |
LitVar | rs41338947 |
Map | rs41338947 |
PheGenI | rs41338947 |
Biobank | rs41338947 |
1000 genomes | rs41338947 |
hgdp | rs41338947 |
ensembl | rs41338947 |
geneview | rs41338947 |
scholar | rs41338947 |
rs41338947 | |
pharmgkb | rs41338947 |
gwascentral | rs41338947 |
openSNP | rs41338947 |
23andMe | rs41338947 |
SNPshot | rs41338947 |
SNPdbe | rs41338947 |
MSV3d | rs41338947 |
GWAS Ctlg | rs41338947 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41338947(A;A) |
Alt | rs41338947(A;A) |
Reference | Rs41338947(C;C) |
Significance | Other |
Disease | HEMOGLOBIN DALLAS |
Variation | info |
Gene | HBA2 |
CLNDBN | HEMOGLOBIN DALLAS |
Reversed | 0 |
HGVS | NC_000016.9:g.223322C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000017012.1, |
[PMID 7803274] The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.