rs2001181
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2001181(C;T) |
Make rs2001181(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31269221 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs2001181 |
dbSNP (classic) | rs2001181 |
ClinGen | rs2001181 |
ebi | rs2001181 |
HLI | rs2001181 |
Exac | rs2001181 |
Gnomad | rs2001181 |
Varsome | rs2001181 |
LitVar | rs2001181 |
Map | rs2001181 |
PheGenI | rs2001181 |
Biobank | rs2001181 |
1000 genomes | rs2001181 |
hgdp | rs2001181 |
ensembl | rs2001181 |
geneview | rs2001181 |
scholar | rs2001181 |
rs2001181 | |
pharmgkb | rs2001181 |
gwascentral | rs2001181 |
openSNP | rs2001181 |
23andMe | rs2001181 |
SNPshot | rs2001181 |
SNPdbe | rs2001181 |
MSV3d | rs2001181 |
GWAS Ctlg | rs2001181 |
GMAF | 0.1281 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2001181(T;T) |
Alt | rs2001181(T;T) |
Reference | Rs2001181(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31236998C; NC_000006.11:g.31236998C>T |
CLNSRC | |
CLNACC |