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: rs3733402
rs3733402
5 1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 0.700 1.000 2 2012 2014
dbSNP: rs11132382
rs11132382
1 4 186222648 intron variant T/G snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs13136536
rs13136536
1 4 186217309 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1511801
rs1511801
1 4 186229556 intron variant A/T snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs1912826
rs1912826
4 4 186228386 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2048
rs2048
1 4 186226979 intron variant G/T snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs28671360
rs28671360
1 4 186257634 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs33930717
rs33930717
1 4 186257634 intron variant -/TGT;TTT delins 0.700 1.000 1 2012 2012
dbSNP: rs35328399
rs35328399
1 4 186217309 intron variant -/GTT delins 0.700 1.000 1 2012 2012
dbSNP: rs35984397
rs35984397
1 4 186240347 intron variant G/A snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs3775298
rs3775298
2 4 186229324 intron variant A/G snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs4241815
rs4241815
1 4 186230988 intron variant C/T snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4241816
rs4241816
1 4 186231173 intron variant A/T snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4241817
rs4241817
1 4 186231504 intron variant T/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4241818
rs4241818
2 4 186232632 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4253236
rs4253236
1 4 186226917 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4253238
rs4253238
4 0.925 0.080 4 186227233 intron variant C/T snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs4253244
rs4253244
1 4 186232621 intron variant C/A snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs4253248
rs4253248
2 4 186234334 intron variant G/A snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4253252
rs4253252
3 4 186236304 intron variant T/G snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4253255
rs4253255
1 4 186237768 intron variant G/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4253256
rs4253256
1 4 186238128 intron variant G/C snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs4253281
rs4253281
1 4 186243195 intron variant G/A snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs4253282
rs4253282
2 4 186243245 intron variant C/T snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs4253294
rs4253294
1 4 186248496 intron variant A/G;T snv 0.700 1.000 1 2012 2012