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: rs2844659
rs2844659 		4 0.851 0.280 6 30856755 intergenic variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2855812
rs2855812
MICB
13 0.790 0.360 6 31504943 intron variant G/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs2857595
rs2857595 		9 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs3094054
rs3094054 		6 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3095089
rs3095089 		3 0.882 0.240 6 30966017 upstream gene variant G/T snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs3099844
rs3099844
MICB-DT
13 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs3115663
rs3115663
PRRC2A ; MIR6832
7 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs3129890
rs3129890 		5 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs3129939
rs3129939
TSBP1 ; TSBP1-AS1
5 0.827 0.360 6 32368989 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs3129963
rs3129963 		4 0.851 0.280 6 32412431 downstream gene variant A/G snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs3130350
rs3130350 		5 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs3130380
rs3130380
HCG18 ; HCG17
10 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs3130473
rs3130473 		6 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs3130544
rs3130544 		10 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs3130564
rs3130564
PSORS1C1
7 0.790 0.360 6 31133897 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs3130618
rs3130618
CSNK2B ; GPANK1
7 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs3131296
rs3131296
NOTCH4
6 0.807 0.320 6 32205216 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs3131379
rs3131379
MSH5 ; MSH5-SAPCD1
10 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs3132580
rs3132580
MUCL3 ; SFTA2 ; HCG21
7 0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs3132610
rs3132610
ABCF1
6 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs3132685
rs3132685
HLA-A ; HCG9
6 0.807 0.320 6 29978172 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3135353
rs3135353 		3 0.882 0.280 6 32425100 intergenic variant C/T snv 9.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs3792783
rs3792783
TNIP1
3 0.882 0.280 5 151076171 intron variant A/G snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs3792785
rs3792785
TNIP1
1 1.000 0.120 5 151072089 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs389884
rs389884
CYP21A2 ; DXO ; STK19
10 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 0.700 1.000 1 2012 2012