Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518849
rs1057518849
EHMT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518874
rs1057518874
SPG11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518943
rs1057518943
IGHMBP2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908096
rs121908096
CYP27A1
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909112
rs121909112
HSPB1
G 0.700 CausalMutation CLINVAR

dbSNP: rs142433332
rs142433332
DARS2
C 0.700 CausalMutation CLINVAR

dbSNP: rs143003434
rs143003434
SPAST
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553201258
rs1553201258
DARS2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553521119
rs1553521119
DYSF
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554781700
rs1554781700
COL5A1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555103652
rs1555103652
GRIN2B
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555889127
rs1555889127
KCNB1 ; LOC105372649
T 0.700 GeneticVariation CLINVAR

dbSNP: rs201689565
rs201689565
SPG11
G 0.700 GeneticVariation CLINVAR

dbSNP: rs201892814
rs201892814
CAPN3
G 0.700 CausalMutation CLINVAR

dbSNP: rs267607261
rs267607261
MPV17
T 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs312262720
rs312262720
SPG11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs368900406
rs368900406
MPV17
C 0.700 GeneticVariation CLINVAR

dbSNP: rs374052333
rs374052333
UBA5 ; NPHP3-ACAD11
T 0.700 GeneticVariation CLINVAR

dbSNP: rs387906686
rs387906686
SCN2A
T 0.700 CausalMutation CLINVAR

dbSNP: rs747900252
rs747900252
COL6A2
A 0.700 CausalMutation CLINVAR

dbSNP: rs758058910
rs758058910
CAPN3
A 0.700 CausalMutation CLINVAR

dbSNP: rs773690764
rs773690764
IGHMBP2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs778768583
rs778768583
CAPN3
C 0.700 CausalMutation CLINVAR