rs41514946
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs41514946(A;A) |
Make rs41514946(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 173573 |
Gene | HBA2 |
is a | snp |
is | mentioned by |
dbSNP | rs41514946 |
dbSNP (classic) | rs41514946 |
ClinGen | rs41514946 |
ebi | rs41514946 |
HLI | rs41514946 |
Exac | rs41514946 |
Gnomad | rs41514946 |
Varsome | rs41514946 |
LitVar | rs41514946 |
Map | rs41514946 |
PheGenI | rs41514946 |
Biobank | rs41514946 |
1000 genomes | rs41514946 |
hgdp | rs41514946 |
ensembl | rs41514946 |
geneview | rs41514946 |
scholar | rs41514946 |
rs41514946 | |
pharmgkb | rs41514946 |
gwascentral | rs41514946 |
openSNP | rs41514946 |
23andMe | rs41514946 |
SNPshot | rs41514946 |
SNPdbe | rs41514946 |
MSV3d | rs41514946 |
GWAS Ctlg | rs41514946 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41514946(A;A) rs41514946(G;G) |
Alt | rs41514946(A;A) rs41514946(G;G) |
Reference | Rs41514946(C;C) |
Significance | Other |
Disease | Hemoglobin Val de Marne |
Variation | info |
Gene | HBA2 |
CLNDBN | Hemoglobin Val de Marne |
Reversed | 0 |
HGVS | NC_000016.9:g.223572C>A |
CLNSRC | HBVAR OMIM Allelic Variant |
CLNACC | RCV000016974.2, |