rs34807671
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs34807671(C;T) |
Make rs34807671(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5253282 |
Gene | HBG2 |
is a | snp |
is | mentioned by |
dbSNP | rs34807671 |
dbSNP (classic) | rs34807671 |
ClinGen | rs34807671 |
ebi | rs34807671 |
HLI | rs34807671 |
Exac | rs34807671 |
Gnomad | rs34807671 |
Varsome | rs34807671 |
LitVar | rs34807671 |
Map | rs34807671 |
PheGenI | rs34807671 |
Biobank | rs34807671 |
1000 genomes | rs34807671 |
hgdp | rs34807671 |
ensembl | rs34807671 |
geneview | rs34807671 |
scholar | rs34807671 |
rs34807671 | |
pharmgkb | rs34807671 |
gwascentral | rs34807671 |
openSNP | rs34807671 |
23andMe | rs34807671 |
SNPshot | rs34807671 |
SNPdbe | rs34807671 |
MSV3d | rs34807671 |
GWAS Ctlg | rs34807671 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs34807671(T;T) |
Alt | rs34807671(T;T) |
Reference | Rs34807671(C;C) |
Significance | Other |
Disease | HEMOGLOBIN F (ONODA) |
Variation | info |
Gene | HBG2 |
CLNDBN | HEMOGLOBIN F (ONODA) |
Reversed | 1 |
HGVS | NC_000011.9:g.5274512G>A |
CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000016128.1, |
[PMID 1703139] Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn.