rs77376497
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs77376497(C;C) |
Make rs77376497(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271620 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs77376497 |
dbSNP (classic) | rs77376497 |
ClinGen | rs77376497 |
ebi | rs77376497 |
HLI | rs77376497 |
Exac | rs77376497 |
Gnomad | rs77376497 |
Varsome | rs77376497 |
LitVar | rs77376497 |
Map | rs77376497 |
PheGenI | rs77376497 |
Biobank | rs77376497 |
1000 genomes | rs77376497 |
hgdp | rs77376497 |
ensembl | rs77376497 |
geneview | rs77376497 |
scholar | rs77376497 |
rs77376497 | |
pharmgkb | rs77376497 |
gwascentral | rs77376497 |
openSNP | rs77376497 |
23andMe | rs77376497 |
SNPshot | rs77376497 |
SNPdbe | rs77376497 |
MSV3d | rs77376497 |
GWAS Ctlg | rs77376497 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77376497(C;C) |
Alt | rs77376497(C;C) |
Reference | Rs77376497(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31239397A>G |
CLNSRC | |
CLNACC |