Gene: INS ×
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: rs121908277
rs121908277
INS ; INS-IGF2
1 1.000 0.080 11 2159877 missense variant T/C snv 0.800 1.000 2 2007 2008
dbSNP: rs80356663
rs80356663
INS ; INS-IGF2
3 0.925 0.120 11 2160901 missense variant G/A;T snv 0.800 1.000 2 2007 2008
dbSNP: rs80356664
rs80356664
INS ; INS-IGF2
5 0.882 0.120 11 2160878 missense variant C/G;T snv 0.800 1.000 2 2007 2008
dbSNP: rs80356666
rs80356666
INS ; INS-IGF2
1 1.000 0.080 11 2160845 missense variant A/C snv 0.800 1.000 2 2007 2008
dbSNP: rs80356667
rs80356667
INS ; INS-IGF2
1 1.000 0.080 11 2160832 missense variant C/A snv 0.800 1.000 2 2007 2008
dbSNP: rs80356668
rs80356668
INS ; INS-IGF2
2 0.925 0.080 11 2160829 missense variant A/C;G snv 0.800 1.000 2 2007 2008
dbSNP: rs80356669
rs80356669
INS ; INS-IGF2
1 1.000 0.080 11 2159920 missense variant G/A snv 0.800 1.000 2 2007 2008
dbSNP: rs80356670
rs80356670
INS ; INS-IGF2
1 1.000 0.080 11 2159917 missense variant C/A snv 0.800 1.000 2 2007 2008
dbSNP: rs80356671
rs80356671
INS ; INS-IGF2
1 1.000 0.080 11 2159898 missense variant C/G;T snv 0.800 1.000 2 2007 2008
dbSNP: rs80356672
rs80356672
INS ; INS-IGF2
2 0.925 0.120 11 2159862 missense variant T/C snv 0.800 1.000 2 2007 2008
dbSNP: rs748749585
rs748749585
INS ; INS-IGF2
1 1.000 0.080 11 2161302 5 prime UTR variant G/A;C;T snv 0.700 1.000 3 2010 2011
dbSNP: rs1135401727
rs1135401727
INS ; INS-IGF2
1 1.000 0.080 11 2161314 5 prime UTR variant GATGGCTGGGGGCTGAGGCTGCAA/- delins 2.1E-05 0.700 1.000 2 2010 2010
dbSNP: rs121908272
rs121908272
INS ; INS-IGF2
1 1.000 0.080 11 2160887 missense variant G/C snv 0.700 1.000 2 2007 2008
dbSNP: rs121908273
rs121908273
INS ; INS-IGF2
1 1.000 0.080 11 2160868 missense variant A/G snv 0.700 1.000 2 2007 2008
dbSNP: rs121908274
rs121908274
INS ; INS-IGF2
2 0.925 0.080 11 2159935 missense variant C/T snv 0.700 1.000 2 2007 2008
dbSNP: rs121908276
rs121908276
INS ; INS-IGF2
1 1.000 0.080 11 2159883 missense variant G/C snv 0.700 1.000 2 2007 2008
dbSNP: rs1554921033
rs1554921033
INS ; INS-IGF2
1 1.000 0.080 11 2161189 5 prime UTR variant T/G snv 0.700 1.000 2 2010 2011
dbSNP: rs1564912403
rs1564912403
INS ; INS-IGF2
1 1.000 0.080 11 2160946 missense variant G/C snv 0.700 0
dbSNP: rs397515519
rs397515519
INS ; INS-IGF2
1 1.000 0.080 11 2159793 synonymous variant T/C snv 4.5E-06 0.700 0
dbSNP: rs397515521
rs397515521
INS ; INS-IGF2
1 1.000 0.080 11 2160969 start lost C/A;T snv 0.700 0
dbSNP: rs797045623
rs797045623
INS ; INS-IGF2
1 1.000 0.080 11 2160028 intron variant C/T snv 0.700 0
dbSNP: rs886041083
rs886041083
INS ; INS-IGF2
1 1.000 0.080 11 2160544 intron variant C/T snv 0.700 0