Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1396171148
rs1396171148
0.851 0.200 2 222613892 missense variant T/G snv
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 0
dbSNP: rs1419129874
rs1419129874
0.851 0.200 2 222642894 missense variant A/G snv 7.0E-06
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 0
dbSNP: rs1466642025
rs1466642025
0.851 0.200 2 222631635 missense variant A/G snv 7.0E-06
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 0
dbSNP: rs1553553086
rs1553553086
0.827 0.280 2 222623699 missense variant C/T snv
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 0
dbSNP: rs1553554543
rs1553554543
0.851 0.200 2 222631606 missense variant T/C snv
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 0