rs35957832
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs35957832(C;C) |
Make rs35957832(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5249729 |
Gene | HBG1 |
is a | snp |
is | mentioned by |
dbSNP | rs35957832 |
dbSNP (classic) | rs35957832 |
ClinGen | rs35957832 |
ebi | rs35957832 |
HLI | rs35957832 |
Exac | rs35957832 |
Gnomad | rs35957832 |
Varsome | rs35957832 |
LitVar | rs35957832 |
Map | rs35957832 |
PheGenI | rs35957832 |
Biobank | rs35957832 |
1000 genomes | rs35957832 |
hgdp | rs35957832 |
ensembl | rs35957832 |
geneview | rs35957832 |
scholar | rs35957832 |
rs35957832 | |
pharmgkb | rs35957832 |
gwascentral | rs35957832 |
openSNP | rs35957832 |
23andMe | rs35957832 |
SNPshot | rs35957832 |
SNPdbe | rs35957832 |
MSV3d | rs35957832 |
GWAS Ctlg | rs35957832 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35957832(C;C) |
Alt | rs35957832(C;C) |
Reference | Rs35957832(G;G) |
Significance | Other |
Disease | HEMOGLOBIN F (XINJIANG) |
Variation | info |
Gene | HBG1 |
CLNDBN | HEMOGLOBIN F (XINJIANG) |
Reversed | 1 |
HGVS | NC_000011.9:g.5270959C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000016167.3, |
[PMID 2448268] Hb F-Xinjiang or A gamma T25(B7)Gly----Arg: a new slow-moving unstable fetal hemoglobin variant.