rs140207606
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs140207606(A;A) |
Make rs140207606(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 88118244 |
Gene | ABCG2 |
is a | snp |
is | mentioned by |
dbSNP | rs140207606 |
dbSNP (classic) | rs140207606 |
ClinGen | rs140207606 |
ebi | rs140207606 |
HLI | rs140207606 |
Exac | rs140207606 |
Gnomad | rs140207606 |
Varsome | rs140207606 |
LitVar | rs140207606 |
Map | rs140207606 |
PheGenI | rs140207606 |
Biobank | rs140207606 |
1000 genomes | rs140207606 |
hgdp | rs140207606 |
ensembl | rs140207606 |
geneview | rs140207606 |
scholar | rs140207606 |
rs140207606 | |
pharmgkb | rs140207606 |
gwascentral | rs140207606 |
openSNP | rs140207606 |
23andMe | rs140207606 |
SNPshot | rs140207606 |
SNPdbe | rs140207606 |
MSV3d | rs140207606 |
GWAS Ctlg | rs140207606 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs140207606(A;A) rs140207606(T;T) |
Alt | rs140207606(A;A) rs140207606(T;T) |
Reference | Rs140207606(G;G) |
Significance | Other |
Disease | Blood group |
Variation | info |
Gene | ABCG2 |
CLNDBN | Blood group, Junior system |
Reversed | 0 |
HGVS | NC_000004.11:g.89039396G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023339.2, |