Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854461
rs137854461
FBN1
C 0.700 CausalMutation CLINVAR

dbSNP: rs137854466
rs137854466
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs137854467
rs137854467
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553212868
rs1553212868
POGZ
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553621496
rs1553621496
UNC80
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554110735
rs1554110735
TFAP2A
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554122802
rs1554122802
FBN2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554699491
rs1554699491
AGTPBP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554700718
rs1554700718
HNRNPK
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555038029
rs1555038029
KMT2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555038111
rs1555038111
KMT2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555397413
rs1555397413
FBN1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555398397
rs1555398397
FBN1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555727493
rs1555727493
KMT2B
TGGCGGCGGCGGCG 0.700 CausalMutation CLINVAR

dbSNP: rs1555968941
rs1555968941
CACNA1C
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1559470315
rs1559470315
CTNNB1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1560755661
rs1560755661
TBCK
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565295267
rs1565295267
MYRF ; TMEM258
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1567263168
rs1567263168
CREBBP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569301036
rs1569301036
TAF1
T 0.700 CausalMutation CLINVAR

dbSNP: rs199564797
rs199564797
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs201943194
rs201943194
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs373145711
rs373145711
ASXL1
T 0.700 CausalMutation CLINVAR

dbSNP: rs376103091
rs376103091
EARS2
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906846
rs387906846
ARID1A
T 0.700 CausalMutation CLINVAR