rs9469220, None

N. diseases: 5
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.
Pemphigus Vulgaris
CUI: C0030809
Disease: Pemphigus Vulgaris
39 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.710 1.000 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.700 1.000 1 2007 2007
Narcolepsy
CUI: C0027404
Disease: Narcolepsy
454 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.700 1.000 1 2009 2009
Pemphigus
CUI: C0030807
Disease: Pemphigus
3 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.700 1.000 1 2019 2019
Pemphigus Foliaceus
CUI: C0263313
Disease: Pemphigus Foliaceus
16 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.010 1.000 1 2019 2019