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: rs11656696
rs11656696
GAS7
5 0.882 0.040 17 10130362 intron variant C/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs12150284
rs12150284
GAS7
3 1.000 0.040 17 10127773 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13227590
rs13227590 		1 7 8111360 upstream gene variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1826598
rs1826598 		1 16 77539058 intergenic variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2025751
rs2025751
PKHD1
2 6 51757651 intron variant T/C snv 0.53 0.700 1.000 1 2014 2014
dbSNP: rs4656461
rs4656461 		7 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 0.700 1.000 1 2014 2014
dbSNP: rs587847
rs587847
LOC105370772
2 15 37367848 intron variant C/A snv 0.69 0.700 1.000 1 2014 2014
dbSNP: rs59072263
rs59072263 		2 7 8112437 upstream gene variant G/T snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs6483184
rs6483184
FAT3
1 11 92655416 intron variant G/C snv 4.9E-03 0.700 1.000 1 2012 2012
dbSNP: rs7518099
rs7518099
TMCO1 ; TMCO1-AS1
4 0.925 0.040 1 165767643 intron variant C/T snv 0.89 0.700 1.000 1 2014 2014
dbSNP: rs7555523
rs7555523
TMCO1
4 0.925 0.040 1 165749742 intron variant C/A snv 0.88 0.700 1.000 1 2012 2012
dbSNP: rs9889528
rs9889528
GAS7
1 17 10132020 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs9913911
rs9913911
GAS7
4 0.925 0.040 17 10127866 intron variant A/G snv 0.32 0.700 1.000 1 2012 2012