Source: ALL
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: rs3809128
rs3809128
12 56316135 non coding transcript exon variant C/T snv 7.2E-03
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2015 2015
dbSNP: rs1330054285
rs1330054285
1.000 0.080 12 56317616 missense variant G/A snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs79824801
rs79824801
1.000 0.040 12 56334353 intron variant T/C snv 4.5E-02
Experimental Organism Basal Cell Carcinoma
Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs79824801
rs79824801
1.000 0.040 12 56334353 intron variant T/C snv 4.5E-02
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
Neoplasms 0.010 1.000 1 2017 2017