Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1010184002
rs1010184002
PEX6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1014959895
rs1014959895
PRMT7
T 0.700 CausalMutation CLINVAR

dbSNP: rs1043679457
rs1043679457
ERCC8
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057518345
rs1057518345
ADNP
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518791
rs1057518791
TRPS1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
POGZ
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518834
rs1057518834
DMD
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518863
rs1057518863
COL7A1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518907
rs1057518907
GNAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518908
rs1057518908
COL2A1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518939
rs1057518939
VPS13B
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518940
rs1057518940
RYR1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518950
rs1057518950
TPO
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519324
rs1057519324
NPR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519334
rs1057519334
NPR2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519338
rs1057519338
AMMECR1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519369
rs1057519369
NF1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1057519370
rs1057519370
NF1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519436
rs1057519436
DHX30
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519451
rs1057519451
NRXN3 ; LOC105370589
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057521737
rs1057521737
EP300
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060505041
rs1060505041
NACC1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1064796765
rs1064796765
DYNC1H1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307135
rs1085307135
PUF60
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307138
rs1085307138
PUF60 ; SCRIB
T 0.700 GeneticVariation CLINVAR