Gene: MECP2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894864
rs104894864
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518718
rs1057518718
MECP2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1064797104
rs1064797104
MECP2
CCTCAGCTTTTCGCTTCCTGCCGGGG 0.700 CausalMutation CLINVAR

dbSNP: rs1557134378
rs1557134378
MECP2
CCACGG 0.700 CausalMutation CLINVAR

dbSNP: rs1557134481
rs1557134481
MECP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557134621
rs1557134621
MECP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557134720
rs1557134720
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557134770
rs1557134770
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557134779
rs1557134779
MECP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557134819
rs1557134819
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557134858
rs1557134858
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557135016
rs1557135016
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135039
rs1557135039
MECP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557135076
rs1557135076
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135110
rs1557135110
MECP2
TGCAAAGAGGAGAAGATGCCCAGAGGAGGCTCACT 0.700 CausalMutation CLINVAR

dbSNP: rs1557135125
rs1557135125
MECP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557135128
rs1557135128
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135137
rs1557135137
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557135197
rs1557135197
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557135212
rs1557135212
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557135213
rs1557135213
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135218
rs1557135218
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557135225
rs1557135225
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557135268
rs1557135268
MECP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557135285
rs1557135285
MECP2
G 0.700 CausalMutation CLINVAR