Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518799
rs1057518799
CUI: C1384666
Disease: hearing impairment
hearing impairment
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
CUI: C4551560
Disease: Truncal obesity
Truncal obesity
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
CUI: C1837084
Disease: Short metacarpal
Short metacarpal
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
CUI: C0349588
Disease: Short stature
Short stature
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518799
rs1057518799
CUI: C0027092
Disease: Myopia
Myopia
TGATTGGCA 0.700 GeneticVariation CLINVAR

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