rs41555616
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41555616(C;G) |
Make rs41555616(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 31271081 |
is a | snp |
is | mentioned by |
dbSNP | rs41555616 |
dbSNP (classic) | rs41555616 |
ClinGen | rs41555616 |
ebi | rs41555616 |
HLI | rs41555616 |
Exac | rs41555616 |
Gnomad | rs41555616 |
Varsome | rs41555616 |
LitVar | rs41555616 |
Map | rs41555616 |
PheGenI | rs41555616 |
Biobank | rs41555616 |
1000 genomes | rs41555616 |
hgdp | rs41555616 |
ensembl | rs41555616 |
geneview | rs41555616 |
scholar | rs41555616 |
rs41555616 | |
pharmgkb | rs41555616 |
gwascentral | rs41555616 |
openSNP | rs41555616 |
23andMe | rs41555616 |
SNPshot | rs41555616 |
SNPdbe | rs41555616 |
MSV3d | rs41555616 |
GWAS Ctlg | rs41555616 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41555616(G;G) |
Alt | rs41555616(G;G) |
Reference | Rs41555616(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31238859G>C |
CLNSRC | |
CLNACC |