rs104895506
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104895506(C;T) |
Make rs104895506(T;T) |
Reference | GRCh37 37.1/132 |
Chromosome | 19 |
Position | 54938096 |
Gene | NCR1, NLRP7 |
is a | snp |
is | mentioned by |
dbSNP | rs104895506 |
dbSNP (classic) | rs104895506 |
ClinGen | rs104895506 |
ebi | rs104895506 |
HLI | rs104895506 |
Exac | rs104895506 |
Gnomad | rs104895506 |
Varsome | rs104895506 |
LitVar | rs104895506 |
Map | rs104895506 |
PheGenI | rs104895506 |
Biobank | rs104895506 |
1000 genomes | rs104895506 |
hgdp | rs104895506 |
ensembl | rs104895506 |
geneview | rs104895506 |
scholar | rs104895506 |
rs104895506 | |
pharmgkb | rs104895506 |
gwascentral | rs104895506 |
openSNP | rs104895506 |
23andMe | rs104895506 |
SNPshot | rs104895506 |
SNPdbe | rs104895506 |
MSV3d | rs104895506 |
GWAS Ctlg | rs104895506 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104895506(A;A) rs104895506(T;T) |
Alt | rs104895506(A;A) rs104895506(T;T) |
Reference | Rs104895506(C;C) |
Significance | Pathogenic |
Disease | Hydatidiform mole |
Variation | info |
Gene | NLRP7 |
CLNDBN | Hydatidiform mole |
Reversed | 1 |
HGVS | NC_000019.9:g.55449464G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000001653.5, |
[PMID 16462743] Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.