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: rs1130183
rs1130183
0.827 0.160 1 160041722 missense variant G/A snv 4.6E-02 4.7E-02
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs1186688
rs1186688
1.000 0.040 1 160055093 intron variant T/C snv 0.41
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs12133079
rs12133079
1.000 0.040 1 160046674 intron variant C/A snv 0.13
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs17375748
rs17375748
1.000 0.040 1 160040361 3 prime UTR variant C/G;T snv
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017