Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs1559470315
rs1559470315
CTNNB1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1562114190
rs1562114190
PHIP ; IRAK1BP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1562127631
rs1562127631
PHIP ; IRAK1BP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569301036
rs1569301036
TAF1
T 0.700 CausalMutation CLINVAR

dbSNP: rs199469465
rs199469465
SRCAP
T 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs368869806
rs368869806
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs542489955
rs542489955
FKBP14 ; LOC105375215
TG 0.700 CausalMutation CLINVAR

dbSNP: rs72645347
rs72645347
COL1A1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs727503054
rs727503054
FBN1
G 0.700 CausalMutation CLINVAR

dbSNP: rs74799832
rs74799832
RET
C 0.700 CausalMutation CLINVAR

dbSNP: rs761857514
rs761857514
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs770374710
rs770374710
MAGEL2
TG 0.700 CausalMutation CLINVAR

dbSNP: rs781565158
rs781565158
PYROXD1
G 0.700 CausalMutation CLINVAR

dbSNP: rs796052505
rs796052505
GABRG2
A 0.700 CausalMutation CLINVAR

dbSNP: rs797045283
rs797045283
ARID1B
T 0.700 CausalMutation CLINVAR

dbSNP: rs864321670
rs864321670
ALDH18A1
T 0.700 CausalMutation CLINVAR

dbSNP: rs869312697
rs869312697
ARID1B
T 0.700 CausalMutation CLINVAR

dbSNP: rs876661151
rs876661151
GRIN2B ; LOC105369668
T 0.700 CausalMutation CLINVAR

dbSNP: rs886040971
rs886040971
TRPS1
A 0.700 CausalMutation CLINVAR