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: rs749125777
rs749125777
1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06
CUI: C0332563
Disease: Papule
Papule
0.700 0
dbSNP: rs749125777
rs749125777
1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal
0.700 0
dbSNP: rs749125777
rs749125777
1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06
CUI: C0241148
Disease: Cutaneous plaque
Cutaneous plaque
0.700 0
dbSNP: rs749125777
rs749125777
1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06
CUI: C0033847
Disease: Pseudoxanthoma Elasticum
Pseudoxanthoma Elasticum
0.700 0
dbSNP: rs749125777
rs749125777
1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06
CUI: C0035317
Disease: Retinal Hemorrhage
Retinal Hemorrhage
0.700 0
dbSNP: rs749125777
rs749125777
1.000 0.160 16 16173287 missense variant G/A;C snv 4.0E-06; 8.0E-06
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris
0.700 0