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: rs104894478
rs104894478
SIX1 ; MIR9718
3 0.882 0.160 14 60648804 missense variant T/C snv 4.0E-06 0.800 1.000 6 2004 2013
dbSNP: rs121909770
rs121909770
SIX1 ; MIR9718
1 1.000 0.040 14 60648826 missense variant A/T snv 0.800 1.000 6 2004 2013
dbSNP: rs80356459
rs80356459
SIX1 ; MIR9718
1 1.000 0.040 14 60648862 missense variant G/A snv 0.800 1.000 6 2004 2013
dbSNP: rs397515560
rs397515560
SIX1 ; MIR9718
1 1.000 0.040 14 60648873 missense variant A/C snv 0.700 1.000 6 2004 2013
dbSNP: rs397515561
rs397515561
SIX1 ; MIR9718
1 1.000 0.040 14 60648856 missense variant G/A snv 0.700 1.000 6 2004 2013
dbSNP: rs397515562
rs397515562
SIX1 ; MIR9718
1 1.000 0.040 14 60649140 missense variant A/T snv 0.700 1.000 6 2004 2013
dbSNP: rs1060499595
rs1060499595
SIX1 ; MIR9718
2 0.925 0.160 14 60648730 stop gained T/A snv 0.700 0
dbSNP: rs1064794308
rs1064794308
SIX1 ; MIR9718
1 1.000 0.040 14 60648861 missense variant C/T snv 0.700 0
dbSNP: rs863223330
rs863223330
SIX1 ; MIR9718
8 0.807 0.280 14 60648629 splice donor variant C/G snv 0.700 0