rs35993097
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs35993097(A;A) |
Make rs35993097(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 176772 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs35993097 |
dbSNP (classic) | rs35993097 |
ClinGen | rs35993097 |
ebi | rs35993097 |
HLI | rs35993097 |
Exac | rs35993097 |
Gnomad | rs35993097 |
Varsome | rs35993097 |
LitVar | rs35993097 |
Map | rs35993097 |
PheGenI | rs35993097 |
Biobank | rs35993097 |
1000 genomes | rs35993097 |
hgdp | rs35993097 |
ensembl | rs35993097 |
geneview | rs35993097 |
scholar | rs35993097 |
rs35993097 | |
pharmgkb | rs35993097 |
gwascentral | rs35993097 |
openSNP | rs35993097 |
23andMe | rs35993097 |
SNPshot | rs35993097 |
SNPdbe | rs35993097 |
MSV3d | rs35993097 |
GWAS Ctlg | rs35993097 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35993097(A;A) |
Alt | rs35993097(A;A) |
Reference | Rs35993097(G;G) |
Significance | Other |
Disease | HEMOGLOBIN AL-AIN ABU DHABI |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN AL-AIN ABU DHABI |
Reversed | 0 |
HGVS | NC_000016.9:g.226771G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017195.2, |
[PMID 1428941] HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family.