rs33958088
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(CT;CT) | 0 | common in clinvar |
Make rs33958088(A;A) |
Make rs33958088(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5226937 |
Gene | HBB |
is a | snp |
is | mentioned by |
dbSNP | rs33958088 |
dbSNP (classic) | rs33958088 |
ClinGen | rs33958088 |
ebi | rs33958088 |
HLI | rs33958088 |
Exac | rs33958088 |
Gnomad | rs33958088 |
Varsome | rs33958088 |
LitVar | rs33958088 |
Map | rs33958088 |
PheGenI | rs33958088 |
Biobank | rs33958088 |
1000 genomes | rs33958088 |
hgdp | rs33958088 |
ensembl | rs33958088 |
geneview | rs33958088 |
scholar | rs33958088 |
rs33958088 | |
pharmgkb | rs33958088 |
gwascentral | rs33958088 |
openSNP | rs33958088 |
23andMe | rs33958088 |
SNPshot | rs33958088 |
SNPdbe | rs33958088 |
MSV3d | rs33958088 |
GWAS Ctlg | rs33958088 |
Merged from | Rs121909828 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs33958088(A;A) rs33958088(T;T) |
Alt | rs33958088(A;A) rs33958088(T;T) |
Reference | Rs33958088(C;C) |
Significance | Other |
Disease | HEMOGLOBIN CHILE |
Variation | info |
Gene | HBB |
CLNDBN | HEMOGLOBIN CHILE |
Reversed | 1 |
HGVS | NC_000011.9:g.5248167G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000016835.2, |