rs35252931
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs35252931(C;C) |
Make rs35252931(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177005 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs35252931 |
dbSNP (classic) | rs35252931 |
ClinGen | rs35252931 |
ebi | rs35252931 |
HLI | rs35252931 |
Exac | rs35252931 |
Gnomad | rs35252931 |
Varsome | rs35252931 |
LitVar | rs35252931 |
Map | rs35252931 |
PheGenI | rs35252931 |
Biobank | rs35252931 |
1000 genomes | rs35252931 |
hgdp | rs35252931 |
ensembl | rs35252931 |
geneview | rs35252931 |
scholar | rs35252931 |
rs35252931 | |
pharmgkb | rs35252931 |
gwascentral | rs35252931 |
openSNP | rs35252931 |
23andMe | rs35252931 |
SNPshot | rs35252931 |
SNPdbe | rs35252931 |
MSV3d | rs35252931 |
GWAS Ctlg | rs35252931 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35252931(C;C) |
Alt | rs35252931(C;C) |
Reference | Rs35252931(G;G) |
Significance | Other |
Disease | HEMOGLOBIN L (PERSIAN GULF) |
Variation | info |
Gene | HBA1 |
CLNDBN | HEMOGLOBIN L (PERSIAN GULF) |
Reversed | 0 |
HGVS | NC_000016.9:g.227004G>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017092.2, |
[PMID 4982774] Haemoglobin L Persian Gulf: alpha-57 (E6) glycine leads to arginine.