Gene: MECP2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28934905
rs28934905
MECP2
G 0.810 CausalMutation CLINVAR

dbSNP: rs61748390
rs61748390
MECP2
C 0.810 CausalMutation CLINVAR

dbSNP: rs28935168
rs28935168
MECP2
C 0.800 CausalMutation CLINVAR

dbSNP: rs61749715
rs61749715
MECP2
C 0.800 CausalMutation CLINVAR

dbSNP: rs61749715
rs61749715
MECP2
A 0.800 CausalMutation CLINVAR

dbSNP: rs61749723
rs61749723
MECP2
C 0.800 CausalMutation CLINVAR

dbSNP: rs61751443
rs61751443
MECP2
T 0.800 CausalMutation CLINVAR

dbSNP: rs61751449
rs61751449
MECP2
A 0.800 CausalMutation CLINVAR

dbSNP: rs61754421
rs61754421
MECP2
A 0.800 CausalMutation CLINVAR

dbSNP: rs61754452
rs61754452
MECP2
A 0.800 CausalMutation CLINVAR

dbSNP: rs61754453
rs61754453
MECP2
A 0.800 CausalMutation CLINVAR

dbSNP: rs61754453
rs61754453
MECP2
T 0.800 CausalMutation CLINVAR

dbSNP: rs61754453
rs61754453
MECP2
C 0.800 CausalMutation CLINVAR

dbSNP: rs61754457
rs61754457
MECP2
T 0.800 CausalMutation CLINVAR

dbSNP: rs61751364
rs61751364
MECP2
A 0.770 CausalMutation CLINVAR

dbSNP: rs61748421
rs61748421
MECP2
T 0.740 CausalMutation CLINVAR

dbSNP: rs61751362
rs61751362
MECP2
A 0.730 GeneticVariation CLINVAR

dbSNP: rs61749721
rs61749721
MECP2
A 0.720 GeneticVariation CLINVAR

dbSNP: rs61751444
rs61751444
MECP2
A 0.720 GeneticVariation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
C 0.710 CausalMutation CLINVAR

dbSNP: rs267608475
rs267608475
MECP2
T 0.710 CausalMutation CLINVAR

dbSNP: rs267608591
rs267608591
MECP2
A 0.710 CausalMutation CLINVAR

dbSNP: rs28934908
rs28934908
MECP2
A 0.710 GeneticVariation CLINVAR

dbSNP: rs61751367
rs61751367
MECP2
A 0.710 CausalMutation CLINVAR

dbSNP: rs786205045
rs786205045
MECP2
A 0.710 CausalMutation CLINVAR