rs378299, ICOSLG

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alopecia
CUI: C0002170
Disease: Alopecia
375 0.882 0.160 21 44241460 upstream gene variant C/T snv 0.010 1.000 1 2014 2014
SVEINSSON CHORIORETINAL ATROPHY
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
30 0.882 0.160 21 44241460 upstream gene variant C/T snv 0.010 1.000 1 2014 2014
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.882 0.160 21 44241460 upstream gene variant C/T snv 0.010 1.000 1 2018 2018