rs63751116
From SNPedia
Merged into | rs35654345 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs63751116(A;A) |
Make rs63751116(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 177323 |
Gene | HBA1 |
is a | snp |
is | mentioned by |
dbSNP | rs63751116 |
dbSNP (classic) | rs63751116 |
ClinGen | rs63751116 |
ebi | rs63751116 |
HLI | rs63751116 |
Exac | rs63751116 |
Gnomad | rs63751116 |
Varsome | rs63751116 |
LitVar | rs63751116 |
Map | rs63751116 |
PheGenI | rs63751116 |
Biobank | rs63751116 |
1000 genomes | rs63751116 |
hgdp | rs63751116 |
ensembl | rs63751116 |
geneview | rs63751116 |
scholar | rs63751116 |
rs63751116 | |
pharmgkb | rs63751116 |
gwascentral | rs63751116 |
openSNP | rs63751116 |
23andMe | rs63751116 |
SNPshot | rs63751116 |
SNPdbe | rs63751116 |
MSV3d | rs63751116 |
GWAS Ctlg | rs63751116 |
Status | Merged into rs35654345 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs63751116(A;A) |
Alt | rs63751116(A;A) |
Reference | Rs63751116(T;T) |
Significance | Untested |
Disease | |
Variation | info |
Gene | HBA1 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000016.9:g.227322T>A |
CLNSRC | |
CLNACC |