rs104894688
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104894688(C;T) |
Make rs104894688(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 48750456 |
Gene | FUT1 |
is a | snp |
is | mentioned by |
dbSNP | rs104894688 |
dbSNP (classic) | rs104894688 |
ClinGen | rs104894688 |
ebi | rs104894688 |
HLI | rs104894688 |
Exac | rs104894688 |
Gnomad | rs104894688 |
Varsome | rs104894688 |
LitVar | rs104894688 |
Map | rs104894688 |
PheGenI | rs104894688 |
Biobank | rs104894688 |
1000 genomes | rs104894688 |
hgdp | rs104894688 |
ensembl | rs104894688 |
geneview | rs104894688 |
scholar | rs104894688 |
rs104894688 | |
pharmgkb | rs104894688 |
gwascentral | rs104894688 |
openSNP | rs104894688 |
23andMe | rs104894688 |
SNPshot | rs104894688 |
SNPdbe | rs104894688 |
MSV3d | rs104894688 |
GWAS Ctlg | rs104894688 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104894688(T;T) |
Alt | rs104894688(T;T) |
Reference | Rs104894688(C;C) |
Significance | Pathogenic |
Disease | Para-Bombay phenotype |
Variation | info |
Gene | FUT1 |
CLNDBN | Para-Bombay phenotype |
Reversed | 1 |
HGVS | NC_000019.9:g.49253713G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000012924.17, |