rs3745635
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs3745635(A;A) |
Make rs3745635(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 5844332 |
Gene | FUT3 |
is a | snp |
is | mentioned by |
dbSNP | rs3745635 |
dbSNP (classic) | rs3745635 |
ClinGen | rs3745635 |
ebi | rs3745635 |
HLI | rs3745635 |
Exac | rs3745635 |
Gnomad | rs3745635 |
Varsome | rs3745635 |
LitVar | rs3745635 |
Map | rs3745635 |
PheGenI | rs3745635 |
Biobank | rs3745635 |
1000 genomes | rs3745635 |
hgdp | rs3745635 |
ensembl | rs3745635 |
geneview | rs3745635 |
scholar | rs3745635 |
rs3745635 | |
pharmgkb | rs3745635 |
gwascentral | rs3745635 |
openSNP | rs3745635 |
23andMe | rs3745635 |
SNPshot | rs3745635 |
SNPdbe | rs3745635 |
MSV3d | rs3745635 |
GWAS Ctlg | rs3745635 |
GMAF | 0.1382 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs3745635(A;A) |
Alt | rs3745635(A;A) |
Reference | Rs3745635(G;G) |
Significance | Other |
Disease | Le(-) PHENOTYPE |
Variation | info |
Gene | FUT3 |
CLNDBN | Le(-) PHENOTYPE |
Reversed | 1 |
HGVS | NC_000019.9:g.5844343C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019289.23, |