Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C0040147
Disease: Thyroiditis
Thyroiditis
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C1835884
Disease: Triangular face
Triangular face
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C1837108
Disease: Decreased muscle mass
Decreased muscle mass
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C4022143
Disease: Unilateral cleft palate
Unilateral cleft palate
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C1856872
Disease: Down-sloping shoulders
Down-sloping shoulders
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs
0.700 0
dbSNP: rs1364709483
rs1364709483
0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05
CUI: C0392006
Disease: Unilateral cleft lip
Unilateral cleft lip
0.700 0