rs1071649
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1071649(A;A) |
Make rs1071649(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271337 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs1071649 |
dbSNP (classic) | rs1071649 |
ClinGen | rs1071649 |
ebi | rs1071649 |
HLI | rs1071649 |
Exac | rs1071649 |
Gnomad | rs1071649 |
Varsome | rs1071649 |
LitVar | rs1071649 |
Map | rs1071649 |
PheGenI | rs1071649 |
Biobank | rs1071649 |
1000 genomes | rs1071649 |
hgdp | rs1071649 |
ensembl | rs1071649 |
geneview | rs1071649 |
scholar | rs1071649 |
rs1071649 | |
pharmgkb | rs1071649 |
gwascentral | rs1071649 |
openSNP | rs1071649 |
23andMe | rs1071649 |
SNPshot | rs1071649 |
SNPdbe | rs1071649 |
MSV3d | rs1071649 |
GWAS Ctlg | rs1071649 |
GMAF | 0.2043 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1071649(A;A) rs1071649(T;T) |
Alt | rs1071649(A;A) rs1071649(T;T) |
Reference | Rs1071649(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31239114G>A; NC_000006.11:g.31239114G>T |
CLNSRC | |
CLNACC |