Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895502
rs104895502
T 0.800 CausalMutation CLINVAR

dbSNP: rs104895502
rs104895502
0.800 GeneticVariation UNIPROT

dbSNP: rs104895502
rs104895502
G 0.800 CausalMutation CLINVAR

dbSNP: rs104895503
rs104895503
C 0.800 CausalMutation CLINVAR

dbSNP: rs104895503
rs104895503
0.800 GeneticVariation UNIPROT

dbSNP: rs104895506
rs104895506
0.800 GeneticVariation UNIPROT

dbSNP: rs104895548
rs104895548
C 0.800 CausalMutation CLINVAR

dbSNP: rs104895548
rs104895548
0.800 GeneticVariation UNIPROT

dbSNP: rs104895549
rs104895549
0.800 GeneticVariation UNIPROT

dbSNP: rs104895549
rs104895549
A 0.800 CausalMutation CLINVAR

dbSNP: rs104895504
rs104895504
T 0.700 CausalMutation CLINVAR

dbSNP: rs104895505
rs104895505
T 0.700 CausalMutation CLINVAR

dbSNP: rs104895525
rs104895525
0.700 GeneticVariation UNIPROT

dbSNP: rs104895530
rs104895530
A 0.700 CausalMutation CLINVAR

dbSNP: rs104895550
rs104895550
0.700 GeneticVariation UNIPROT

dbSNP: rs104895552
rs104895552
0.700 GeneticVariation UNIPROT

dbSNP: rs104895553
rs104895553
TC 0.700 CausalMutation CLINVAR

dbSNP: rs104895554
rs104895554
G 0.700 CausalMutation CLINVAR

dbSNP: rs104895506
rs104895506
A 0.800 CausalMutation CLINVAR Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans. 16462743

2006

dbSNP: rs104895512
rs104895512
C 0.700 CausalMutation CLINVAR A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles. 18039680

2008

dbSNP: rs104895506
rs104895506
A 0.800 CausalMutation CLINVAR Homozygous NLRP7 mutations in a Moroccan woman with recurrent reproductive failure. 19054016

2009

dbSNP: rs104895506
rs104895506
A 0.800 CausalMutation CLINVAR Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region. 19246479

2009

dbSNP: rs104895512
rs104895512
C 0.700 CausalMutation CLINVAR NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation. 19066229

2009

dbSNP: rs104895506
rs104895506
A 0.800 CausalMutation CLINVAR NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage. 21659348

2011

dbSNP: rs104895506
rs104895506
A 0.800 CausalMutation CLINVAR Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles. 22315435

2012