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

dbSNP: rs1057518718
rs1057518718
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499620
rs1060499620
GCT 0.700 CausalMutation CLINVAR Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome. 23696494

2013

dbSNP: rs1060499621
rs1060499621
G 0.700 CausalMutation CLINVAR Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome. 23696494

2013

dbSNP: rs1064792898
rs1064792898
T 0.700 CausalMutation CLINVAR Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome. 23696494

2013

dbSNP: rs1064792899
rs1064792899
A 0.700 GeneticVariation CLINVAR Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome. 23696494

2013

dbSNP: rs1064797104
rs1064797104
CCTCAGCTTTTCGCTTCCTGCCGGGG 0.700 CausalMutation CLINVAR

dbSNP: rs1557134378
rs1557134378
CCACGG 0.700 CausalMutation CLINVAR

dbSNP: rs1557134481
rs1557134481
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557134621
rs1557134621
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557134720
rs1557134720
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557134770
rs1557134770
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557134779
rs1557134779
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557134819
rs1557134819
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557134858
rs1557134858
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557135016
rs1557135016
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135039
rs1557135039
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557135076
rs1557135076
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135110
rs1557135110
TGCAAAGAGGAGAAGATGCCCAGAGGAGGCTCACT 0.700 CausalMutation CLINVAR

dbSNP: rs1557135125
rs1557135125
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557135128
rs1557135128
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557135137
rs1557135137
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557135197
rs1557135197
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557135212
rs1557135212
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557135213
rs1557135213
C 0.700 CausalMutation CLINVAR