rs767222404
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs767222404(A;A) |
Make rs767222404(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 19 |
Position | 2993574 |
Gene | TLE6 |
is a | snp |
is | mentioned by |
dbSNP | rs767222404 |
dbSNP (classic) | rs767222404 |
ClinGen | rs767222404 |
ebi | rs767222404 |
HLI | rs767222404 |
Exac | rs767222404 |
Gnomad | rs767222404 |
Varsome | rs767222404 |
LitVar | rs767222404 |
Map | rs767222404 |
PheGenI | rs767222404 |
Biobank | rs767222404 |
1000 genomes | rs767222404 |
hgdp | rs767222404 |
ensembl | rs767222404 |
geneview | rs767222404 |
scholar | rs767222404 |
rs767222404 | |
pharmgkb | rs767222404 |
gwascentral | rs767222404 |
openSNP | rs767222404 |
23andMe | rs767222404 |
SNPshot | rs767222404 |
SNPdbe | rs767222404 |
MSV3d | rs767222404 |
GWAS Ctlg | rs767222404 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767222404(A;A) rs767222404(G;G) |
Alt | rs767222404(A;A) rs767222404(G;G) |
Reference | Rs767222404(C;C) |
Significance | Pathogenic |
Disease | Preimplantation embryonic lethality 1 |
Variation | info |
Gene | TLE6 |
CLNDBN | Preimplantation embryonic lethality 1 |
Reversed | 0 |
HGVS | NC_000019.9:g.2993572C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000207476.3, |