rs376664522
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs376664522(A;A) |
Make rs376664522(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 219212413 |
Gene | ABCB6 |
is a | snp |
is | mentioned by |
dbSNP | rs376664522 |
dbSNP (classic) | rs376664522 |
ClinGen | rs376664522 |
ebi | rs376664522 |
HLI | rs376664522 |
Exac | rs376664522 |
Gnomad | rs376664522 |
Varsome | rs376664522 |
LitVar | rs376664522 |
Map | rs376664522 |
PheGenI | rs376664522 |
Biobank | rs376664522 |
1000 genomes | rs376664522 |
hgdp | rs376664522 |
ensembl | rs376664522 |
geneview | rs376664522 |
scholar | rs376664522 |
rs376664522 | |
pharmgkb | rs376664522 |
gwascentral | rs376664522 |
openSNP | rs376664522 |
23andMe | rs376664522 |
SNPshot | rs376664522 |
SNPdbe | rs376664522 |
MSV3d | rs376664522 |
GWAS Ctlg | rs376664522 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376664522(A;A) |
Alt | rs376664522(A;A) |
Reference | Rs376664522(G;G) |
Significance | Other |
Disease | Langereis blood group |
Variation | info |
Gene | ABCB6 |
CLNDBN | Langereis blood group |
Reversed | 0 |
HGVS | NC_000002.11:g.220077135G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023436.3, |