rs77665001
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs77665001(A;A) |
Make rs77665001(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355485 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs77665001 |
dbSNP (classic) | rs77665001 |
ClinGen | rs77665001 |
ebi | rs77665001 |
HLI | rs77665001 |
Exac | rs77665001 |
Gnomad | rs77665001 |
Varsome | rs77665001 |
LitVar | rs77665001 |
Map | rs77665001 |
PheGenI | rs77665001 |
Biobank | rs77665001 |
1000 genomes | rs77665001 |
hgdp | rs77665001 |
ensembl | rs77665001 |
geneview | rs77665001 |
scholar | rs77665001 |
rs77665001 | |
pharmgkb | rs77665001 |
gwascentral | rs77665001 |
openSNP | rs77665001 |
23andMe | rs77665001 |
SNPshot | rs77665001 |
SNPdbe | rs77665001 |
MSV3d | rs77665001 |
GWAS Ctlg | rs77665001 |
GMAF | 0.06107 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77665001(A;A) rs77665001(C;C) |
Alt | rs77665001(A;A) rs77665001(C;C) |
Reference | Rs77665001(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31323262G>C |
CLNSRC | |
CLNACC |