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: rs10761779
rs10761779
JMJD1C
3 10 63515167 intron variant A/G snv 0.42 0.700 1.000 1 2008 2008
dbSNP: rs11597390
rs11597390 		4 10 100101678 downstream gene variant G/A snv 0.29 0.700 1.000 1 2008 2008
dbSNP: rs1169313
rs1169313
C12orf43
6 12 121004867 intron variant T/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs12355784
rs12355784
JMJD1C
3 10 63361805 intron variant C/A;T snv 0.700 1.000 1 2008 2008
dbSNP: rs1780324
rs1780324 		3 1 21495264 intergenic variant A/G snv 0.48 0.700 1.000 1 2008 2008
dbSNP: rs2281135
rs2281135
PNPLA3
10 0.851 0.160 22 43936690 intron variant G/A snv 0.19 0.700 1.000 1 2008 2008
dbSNP: rs4820599
rs4820599
GGT1 ; LRRC75B
6 0.925 0.160 22 24594246 intron variant A/G snv 0.43 0.700 1.000 1 2008 2008
dbSNP: rs4962153
rs4962153
ADAMTS13 ; CACFD1
9 0.925 0.120 9 133458632 intron variant A/G snv 0.79 0.700 1.000 1 2008 2008
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs9467160
rs9467160
GPLD1
3 6 24441518 intron variant G/A snv 0.29 0.700 1.000 1 2008 2008