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: rs183671
rs183671
1.000 0.040 5 33964105 intron variant T/A;G snv
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
0.700 1.000 2 2015 2018
dbSNP: rs35412
rs35412
5 33967040 intron variant C/G snv 0.81
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
0.700 1.000 1 2015 2015
dbSNP: rs16891982
rs16891982
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
0.800 1.000 3 2007 2018