rs34988734
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs34988734(C;T) |
Make rs34988734(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177101 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs34988734 |
dbSNP (classic) | rs34988734 |
ClinGen | rs34988734 |
ebi | rs34988734 |
HLI | rs34988734 |
Exac | rs34988734 |
Gnomad | rs34988734 |
Varsome | rs34988734 |
LitVar | rs34988734 |
Map | rs34988734 |
PheGenI | rs34988734 |
Biobank | rs34988734 |
1000 genomes | rs34988734 |
hgdp | rs34988734 |
ensembl | rs34988734 |
geneview | rs34988734 |
scholar | rs34988734 |
rs34988734 | |
pharmgkb | rs34988734 |
gwascentral | rs34988734 |
openSNP | rs34988734 |
23andMe | rs34988734 |
SNPshot | rs34988734 |
SNPdbe | rs34988734 |
MSV3d | rs34988734 |
GWAS Ctlg | rs34988734 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34988734(T;T) |
Alt | rs34988734(T;T) |
Reference | Rs34988734(C;C) |
Significance | Other |
Disease | HEMOGLOBIN VILLEURBANNE |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN VILLEURBANNE |
Reversed | 0 |
HGVS | NC_000016.9:g.227100C>T |
CLNSRC | HBVAR OMIM Allelic Variant |
CLNACC | RCV000017232.2, |
[PMID 9269086] Combined mass spectrometric methods for the characterization of human hemoglobin variants localized within alpha T9 peptide: identification of Hb Villeurbanne alpha 89 (FG1) His-->Tyr.