Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895512
rs104895512
NCR1 ; NLRP7
C 0.700 CausalMutation CLINVAR The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss. 23354651

2013
dbSNP: rs104895512
rs104895512
NCR1 ; NLRP7
C 0.700 CausalMutation CLINVAR NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation. 19066229

2009
dbSNP: rs104895512
rs104895512
NCR1 ; NLRP7
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