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: rs121912875
rs121912875
1 1.000 0.080 12 47979519 missense variant C/A snv 0.800 1.000 2 1995 2005
dbSNP: rs121912880
rs121912880
4 0.882 0.080 12 47986353 missense variant C/A;T snv 0.800 1.000 2 1995 2005
dbSNP: rs121912881
rs121912881
1 1.000 0.080 12 47986388 missense variant C/A snv 0.800 1.000 2 1995 2005
dbSNP: rs121912895
rs121912895
1 1.000 0.080 12 47978320 missense variant T/C snv 0.800 1.000 2 1995 2005
dbSNP: rs1064795155
rs1064795155
FN1
1 1.000 0.080 2 215428331 missense variant G/C snv 0.700 0
dbSNP: rs1181638652
rs1181638652
FN1
2 0.925 0.160 2 215430725 missense variant G/A;C snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs121912871
rs121912871
1 1.000 0.080 12 47989769 missense variant C/T snv 0.700 0
dbSNP: rs121912874
rs121912874
14 0.716 0.400 12 47978329 missense variant G/A snv 0.700 0
dbSNP: rs121912893
rs121912893
15 0.708 0.400 12 47983721 stop gained G/A;T snv 0.700 0
dbSNP: rs1441937959
rs1441937959
20 0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 0.700 0
dbSNP: rs1553658926
rs1553658926
FN1
2 0.925 0.160 2 215428246 missense variant A/C snv 0.700 0
dbSNP: rs1553659131
rs1553659131
FN1
2 0.925 0.160 2 215428306 missense variant A/C snv 0.700 0
dbSNP: rs1553667072
rs1553667072
FN1
3 0.882 0.200 2 215433372 missense variant A/G snv 0.700 0
dbSNP: rs1553669703
rs1553669703
2 0.925 0.160 2 215434713 missense variant C/A snv 0.700 0
dbSNP: rs1559604072
rs1559604072
FN1
1 1.000 0.080 2 215430762 missense variant C/T snv 0.700 0
dbSNP: rs1559609410
rs1559609410
FN1
1 1.000 0.080 2 215431874 missense variant C/T snv 0.700 0
dbSNP: rs1559616744
rs1559616744
FN1
1 1.000 0.080 2 215433371 missense variant C/T snv 0.700 0
dbSNP: rs794727261
rs794727261
14 0.716 0.400 12 47999953 stop gained G/T snv 0.700 0
dbSNP: rs111033553
rs111033553
2 0.925 0.080 6 116120332 missense variant C/T snv 0.010 1.000 1 1998 1998