Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10045431
rs10045431 		4 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.010 1.000 1 2014 2014
dbSNP: rs1020856343
rs1020856343
SLC22A5
5 0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1050152
rs1050152
SLC22A4 ; MIR3936HG
10 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2005 2005
dbSNP: rs2241880
rs2241880
ATG16L1 ; SCARNA5
37 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2014 2014
dbSNP: rs2276631
rs2276631
SLC11A1
3 0.882 0.120 2 218384290 missense variant C/T snv 0.23 0.23 0.010 1.000 1 2013 2013
dbSNP: rs913143152
rs913143152
ATP8A2
1 1.000 0.080 13 25570800 missense variant C/T snv 0.010 1.000 1 2005 2005