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: rs12220777
rs12220777 		2 1.000 0.040 10 80028348 upstream gene variant T/C snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs1265093
rs1265093
PSORS1C1 ; PSORS1C2
2 1.000 0.040 6 31139410 non coding transcript exon variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1923539
rs1923539 		2 1.000 0.040 10 79935194 intron variant G/A snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs2074488
rs2074488
HLA-B ; HLA-C
3 0.925 0.160 6 31272654 intron variant G/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs3130559
rs3130559
PSORS1C1
3 0.925 0.160 6 31129524 intron variant C/T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs3851050
rs3851050 		2 1.000 0.040 10 80122614 upstream gene variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs3923564
rs3923564
SFTPD
2 1.000 0.040 10 79976225 intron variant A/G snv 5.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs6585424
rs6585424
ANXA11
2 1.000 0.040 10 80173992 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs7078012
rs7078012
SFTPD
2 1.000 0.040 10 79945677 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs728616
rs728616
TMEM254
2 1.000 0.040 10 80088158 intron variant G/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs8048576
rs8048576
ATP2C2
2 1.000 0.040 16 84389428 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9266629
rs9266629 		2 1.000 0.040 6 31379045 upstream gene variant T/C snv 0.15 0.700 1.000 1 2012 2012