rs771075821
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs771075821(A;A) |
Make rs771075821(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 17476705 |
Gene | ABCC8 |
is a | snp |
is | mentioned by |
dbSNP | rs771075821 |
dbSNP (classic) | rs771075821 |
ClinGen | rs771075821 |
ebi | rs771075821 |
HLI | rs771075821 |
Exac | rs771075821 |
Gnomad | rs771075821 |
Varsome | rs771075821 |
LitVar | rs771075821 |
Map | rs771075821 |
PheGenI | rs771075821 |
Biobank | rs771075821 |
1000 genomes | rs771075821 |
hgdp | rs771075821 |
ensembl | rs771075821 |
geneview | rs771075821 |
scholar | rs771075821 |
rs771075821 | |
pharmgkb | rs771075821 |
gwascentral | rs771075821 |
openSNP | rs771075821 |
23andMe | rs771075821 |
SNPshot | rs771075821 |
SNPdbe | rs771075821 |
MSV3d | rs771075821 |
GWAS Ctlg | rs771075821 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs771075821(A;A) rs771075821(T;T) |
Alt | rs771075821(A;A) rs771075821(T;T) |
Reference | Rs771075821(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.17498252G>T |
CLNSRC | |
CLNACC | RCV000201893.1, |