Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853226
rs137853226
GNAI2
T 0.700 CausalMutation CLINVAR

dbSNP: rs137853227
rs137853227
GNAI2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519865
rs1057519865
FOXL2 ; FOXL2NB
0.020 GeneticVariation BEFREE Our findings suggest that FOXL2 p.C134W mutation-positive adult-type GCT of the ovary may not be common in the Japanese as compared to the previous data. 24689977

2014
dbSNP: rs1057519865
rs1057519865
FOXL2 ; FOXL2NB
0.020 GeneticVariation BEFREE Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G). 20098707

2010