rs775156958
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs775156958(A;A) |
Make rs775156958(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 17382046 |
Gene | PADI6 |
is a | snp |
is | mentioned by |
dbSNP | rs775156958 |
dbSNP (classic) | rs775156958 |
ClinGen | rs775156958 |
ebi | rs775156958 |
HLI | rs775156958 |
Exac | rs775156958 |
Gnomad | rs775156958 |
Varsome | rs775156958 |
LitVar | rs775156958 |
Map | rs775156958 |
PheGenI | rs775156958 |
Biobank | rs775156958 |
1000 genomes | rs775156958 |
hgdp | rs775156958 |
ensembl | rs775156958 |
geneview | rs775156958 |
scholar | rs775156958 |
rs775156958 | |
pharmgkb | rs775156958 |
gwascentral | rs775156958 |
openSNP | rs775156958 |
23andMe | rs775156958 |
SNPshot | rs775156958 |
SNPdbe | rs775156958 |
MSV3d | rs775156958 |
GWAS Ctlg | rs775156958 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775156958(A;A) |
Alt | rs775156958(A;A) |
Reference | Rs775156958(T;T) |
Significance | Pathogenic |
Disease | Preimplantation embryonic lethality 2 |
Variation | info |
Gene | PADI6 |
CLNDBN | Preimplantation embryonic lethality 2 |
Reversed | 0 |
HGVS | NC_000001.10:g.17708541T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000412664.1, |