Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1251778848
rs1251778848
KMT2D
A 0.700 CausalMutation CLINVAR

dbSNP: rs139632595
rs139632595
EXOSC9
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553621496
rs1553621496
UNC80
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553770577
rs1553770577
UBA5 ; NPHP3-ACAD11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554700718
rs1554700718
HNRNPK
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555038111
rs1555038111
KMT2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557570794
rs1557570794
ARID1A
AGCCGCCTCCCTCCTCCAGCGCC 0.700 CausalMutation CLINVAR

dbSNP: rs397517077
rs397517077
CBL
C 0.700 GeneticVariation CLINVAR

dbSNP: rs398123009
rs398123009
PACS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs61750420
rs61750420
PEX1
T 0.700 CausalMutation CLINVAR