rs34629158
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs34629158(A;A) |
Make rs34629158(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177313 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs34629158 |
dbSNP (classic) | rs34629158 |
ClinGen | rs34629158 |
ebi | rs34629158 |
HLI | rs34629158 |
Exac | rs34629158 |
Gnomad | rs34629158 |
Varsome | rs34629158 |
LitVar | rs34629158 |
Map | rs34629158 |
PheGenI | rs34629158 |
Biobank | rs34629158 |
1000 genomes | rs34629158 |
hgdp | rs34629158 |
ensembl | rs34629158 |
geneview | rs34629158 |
scholar | rs34629158 |
rs34629158 | |
pharmgkb | rs34629158 |
gwascentral | rs34629158 |
openSNP | rs34629158 |
23andMe | rs34629158 |
SNPshot | rs34629158 |
SNPdbe | rs34629158 |
MSV3d | rs34629158 |
GWAS Ctlg | rs34629158 |
Merged from | Rs63750629 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34629158(A;A) |
Alt | rs34629158(A;A) |
Reference | Rs34629158(G;G) |
Significance | Other |
Disease | HEMOGLOBIN TONOSHO |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN TONOSHO |
Reversed | 0 |
HGVS | NC_000016.9:g.227312G>A |
CLNSRC | HBVAR OMIM Allelic Variant |
CLNACC | RCV000017183.2, |
[PMID 2283295] A new alpha chain variant Hb Tonosho [alpha 110(G17)Ala----Thr]: subunit dissociation during cation exchange chromatography for Hb A1c assay.