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: rs17728461
rs17728461
1 0.776 0.120 22 30202563 intron variant C/G snv 0.25 0.720 1.000 1 2011 2015
dbSNP: rs11090598
rs11090598
1 1.000 0.080 22 30125781 intron variant A/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs12167333
rs12167333
1 1.000 0.080 22 30179823 downstream gene variant C/T snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs1978083
rs1978083
1 1.000 0.080 22 30174454 intron variant C/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs2023683
rs2023683
1 1.000 0.080 22 30203607 intron variant G/A snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs4239933
rs4239933
1 1.000 0.080 22 30116425 intron variant C/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs4337577
rs4337577
1 1.000 0.080 22 30116139 intron variant G/C snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs718772
rs718772
1 0.925 0.120 22 30108218 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs7510705
rs7510705
1 1.000 0.080 22 30097929 intron variant A/G snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs8138286
rs8138286
1 1.000 0.080 22 30166998 intron variant A/C;G snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs8141404
rs8141404
1 1.000 0.080 22 30078227 intron variant C/T snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs8141765
rs8141765
1 1.000 0.080 22 30166250 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9614157
rs9614157
1 1.000 0.080 22 30201821 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs9614158
rs9614158
1 1.000 0.080 22 30201891 intron variant A/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs9614159
rs9614159
1 0.882 0.160 22 30205254 intron variant G/A snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs9620953
rs9620953
1 1.000 0.080 22 30150256 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs9625919
rs9625919
1 1.000 0.080 22 30104969 intron variant G/T snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs9625933
rs9625933
1 1.000 0.080 22 30159227 intron variant G/A snv 0.21 0.700 1.000 1 2011 2011