rs387906908
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AT;AT) | 0 | common in clinvar |
Make rs387906908(-;-) |
Make rs387906908(-;AT) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 219213467 |
Gene | ABCB6 |
is a | snp |
is | mentioned by |
dbSNP | rs387906908 |
dbSNP (classic) | rs387906908 |
ClinGen | rs387906908 |
ebi | rs387906908 |
HLI | rs387906908 |
Exac | rs387906908 |
Gnomad | rs387906908 |
Varsome | rs387906908 |
LitVar | rs387906908 |
Map | rs387906908 |
PheGenI | rs387906908 |
Biobank | rs387906908 |
1000 genomes | rs387906908 |
hgdp | rs387906908 |
ensembl | rs387906908 |
geneview | rs387906908 |
scholar | rs387906908 |
rs387906908 | |
pharmgkb | rs387906908 |
gwascentral | rs387906908 |
openSNP | rs387906908 |
23andMe | rs387906908 |
SNPshot | rs387906908 |
SNPdbe | rs387906908 |
MSV3d | rs387906908 |
GWAS Ctlg | rs387906908 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906908(-;-) |
Alt | rs387906908(-;-) |
Reference | Rs387906908(AT;AT) |
Significance | Other |
Disease | Langereis blood group |
Variation | info |
Gene | ABCB6 |
CLNDBN | Langereis blood group |
Reversed | 1 |
HGVS | NC_000002.11:g.220078189_220078190delAT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023435.4, |