Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057515572
rs1057515572
PMS2
CUI: C1843367
Disease: Poor school performance
Poor school performance 		ACT 0.700 GeneticVariation CLINVAR Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation. 17557300

2007
dbSNP: rs1057517843
rs1057517843
TUBA1A
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518772
rs1057518772
KCNQ2 ; LOC105372721
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518777
rs1057518777
UBE3A ; SNHG14
CUI: C1843367
Disease: Poor school performance
Poor school performance 		AGTATGAGATGTAG 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518781
rs1057518781
MCOLN1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518782
rs1057518782
MCOLN1 ; LOC105372261
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
POGZ
CUI: C1843367
Disease: Poor school performance
Poor school performance 		TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518800
rs1057518800
GRIN2B
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518850
rs1057518850
FMR1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518872
rs1057518872
GJA1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518913
rs1057518913
EHMT1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518913
rs1057518913
EHMT1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518918
rs1057518918
ARID1B
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518926
rs1057518926
FOXP1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518939
rs1057518939
VPS13B
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519381
rs1057519381
MED12
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519389
rs1057519389
EBF3
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. 28017372

2017
dbSNP: rs1057519389
rs1057519389
EBF3
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. 28017372

2017
dbSNP: rs1057519392
rs1057519392
POGZ
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519393
rs1057519393
KDM5C
CUI: C1843367
Disease: Poor school performance
Poor school performance 		CA 0.700 CausalMutation CLINVAR

dbSNP: rs1057519394
rs1057519394
SLC9A6
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519395
rs1057519395
SHANK3
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519398
rs1057519398
SMC1A
CUI: C1843367
Disease: Poor school performance
Poor school performance 		CG 0.700 CausalMutation CLINVAR

dbSNP: rs1057519399
rs1057519399
ANKRD11
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519400
rs1057519400
SYNGAP1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR