Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.420 GermlineCausalMutation disease ORPHANET Messenger RNA levels of SCO2 were significantly downregulated in myopic mouse retinae. 23643385 2013
Entrez Id: 55214
Gene Symbol: P3H2
P3H2 		0.310 GermlineCausalMutation disease ORPHANET High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2. 21885030 2011
Entrez Id: 4043
Gene Symbol: LRPAP1
LRPAP1 		0.310 GermlineCausalMutation disease ORPHANET Mutations in LRPAP1 are associated with severe myopia in humans. 23830514 2013
Entrez Id: 1280
Gene Symbol: COL2A1
COL2A1 		0.420 CausalMutation disease CLINVAR
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.130 CausalMutation disease CLINVAR
Entrez Id: 7299
Gene Symbol: TYR
TYR 		0.110 CausalMutation disease CLINVAR
Entrez Id: 284217
Gene Symbol: LAMA1
LAMA1 		0.110 CausalMutation disease CLINVAR
Entrez Id: 84231
Gene Symbol: TRAF7
TRAF7 		0.100 CausalMutation disease CLINVAR
Entrez Id: 55023
Gene Symbol: PHIP
PHIP 		0.100 CausalMutation disease CLINVAR
Entrez Id: 2475
Gene Symbol: MTOR
MTOR 		0.100 CausalMutation disease CLINVAR
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.100 CausalMutation disease CLINVAR
Entrez Id: 79813
Gene Symbol: EHMT1
EHMT1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 7399
Gene Symbol: USH2A
USH2A 		0.100 CausalMutation disease CLINVAR
Entrez Id: 7046
Gene Symbol: TGFBR1
TGFBR1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 339400
Gene Symbol: FLG-AS1
FLG-AS1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.100 CausalMutation disease CLINVAR
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		0.100 CausalMutation disease CLINVAR
Entrez Id: 2186
Gene Symbol: BPTF
BPTF 		0.100 CausalMutation disease CLINVAR Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features. 28942966 2017
Entrez Id: 54551
Gene Symbol: MAGEL2
MAGEL2 		0.100 CausalMutation disease CLINVAR
Entrez Id: 6925
Gene Symbol: TCF4
TCF4 		0.100 CausalMutation disease CLINVAR
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 7287
Gene Symbol: TULP1
TULP1 		0.100 CausalMutation disease CLINVAR Antioxidant effect of aqueous extract of four plants with therapeutic potential on gynecological diseases; Semen persicae, Leonurus cardiaca, Hedyotis diffusa, and Curcuma zedoaria. 29178942 2017
Entrez Id: 182
Gene Symbol: JAG1
JAG1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B 		0.100 CausalMutation disease CLINVAR
Entrez Id: 79147
Gene Symbol: FKRP
FKRP 		0.100 CausalMutation disease CLINVAR