rs34868036
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs34868036(C;T) |
Make rs34868036(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177110 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs34868036 |
dbSNP (classic) | rs34868036 |
ClinGen | rs34868036 |
ebi | rs34868036 |
HLI | rs34868036 |
Exac | rs34868036 |
Gnomad | rs34868036 |
Varsome | rs34868036 |
LitVar | rs34868036 |
Map | rs34868036 |
PheGenI | rs34868036 |
Biobank | rs34868036 |
1000 genomes | rs34868036 |
hgdp | rs34868036 |
ensembl | rs34868036 |
geneview | rs34868036 |
scholar | rs34868036 |
rs34868036 | |
pharmgkb | rs34868036 |
gwascentral | rs34868036 |
openSNP | rs34868036 |
23andMe | rs34868036 |
SNPshot | rs34868036 |
SNPdbe | rs34868036 |
MSV3d | rs34868036 |
GWAS Ctlg | rs34868036 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34868036(T;T) |
Alt | rs34868036(T;T) |
Reference | Rs34868036(C;C) |
Significance | Other |
Disease | HEMOGLOBIN CEMENELUM |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN CEMENELUM |
Reversed | 0 |
HGVS | NC_000016.9:g.227109C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017205.2, |
[PMID 8148419] Hb Cemenelum [alpha 92 (FG4) Arg-->Trp]: a hemoglobin variant of the alpha 1/beta 2 interface that displays a moderate increase in oxygen affinity.