rs78545099
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs78545099(A;G) |
Make rs78545099(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356708 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs78545099 |
dbSNP (classic) | rs78545099 |
ClinGen | rs78545099 |
ebi | rs78545099 |
HLI | rs78545099 |
Exac | rs78545099 |
Gnomad | rs78545099 |
Varsome | rs78545099 |
LitVar | rs78545099 |
Map | rs78545099 |
PheGenI | rs78545099 |
Biobank | rs78545099 |
1000 genomes | rs78545099 |
hgdp | rs78545099 |
ensembl | rs78545099 |
geneview | rs78545099 |
scholar | rs78545099 |
rs78545099 | |
pharmgkb | rs78545099 |
gwascentral | rs78545099 |
openSNP | rs78545099 |
23andMe | rs78545099 |
SNPshot | rs78545099 |
SNPdbe | rs78545099 |
MSV3d | rs78545099 |
GWAS Ctlg | rs78545099 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs78545099(C;C) rs78545099(G;G) rs78545099(T;T) |
Alt | rs78545099(C;C) rs78545099(G;G) rs78545099(T;T) |
Reference | Rs78545099(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324485T>A; NC_000006.11:g.31324485T>C; NC_000006.11:g.31324485T>G |
CLNSRC | |
CLNACC |