rs34019507
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs34019507(G;T) |
Make rs34019507(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5254409 |
Gene | HBG2 |
is a | snp |
is | mentioned by |
dbSNP | rs34019507 |
dbSNP (classic) | rs34019507 |
ClinGen | rs34019507 |
ebi | rs34019507 |
HLI | rs34019507 |
Exac | rs34019507 |
Gnomad | rs34019507 |
Varsome | rs34019507 |
LitVar | rs34019507 |
Map | rs34019507 |
PheGenI | rs34019507 |
Biobank | rs34019507 |
1000 genomes | rs34019507 |
hgdp | rs34019507 |
ensembl | rs34019507 |
geneview | rs34019507 |
scholar | rs34019507 |
rs34019507 | |
pharmgkb | rs34019507 |
gwascentral | rs34019507 |
openSNP | rs34019507 |
23andMe | rs34019507 |
SNPshot | rs34019507 |
SNPdbe | rs34019507 |
MSV3d | rs34019507 |
GWAS Ctlg | rs34019507 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34019507(C;C) rs34019507(T;T) |
Alt | rs34019507(C;C) rs34019507(T;T) |
Reference | Rs34019507(G;G) |
Significance | Other |
Disease | HEMOGLOBIN F (CLARKE) |
Variation | info |
Gene | HBG2 |
CLNDBN | HEMOGLOBIN F (CLARKE) |
Reversed | 1 |
HGVS | NC_000011.9:g.5275639C>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000016101.1, |
[PMID 2442123] Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.