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: rs2014486
rs2014486
2 1.000 0.040 11 1237573 intron variant A/G snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs2075859
rs2075859
1 11 1229258 missense variant C/G;T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs2672812
rs2672812
1 11 1228142 intron variant G/A snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs2735727
rs2735727
1 11 1236229 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2735733
rs2735733
2 1.000 0.040 11 1240410 intron variant C/T snv 0.49 0.43 0.700 1.000 1 2013 2013
dbSNP: rs2857476
rs2857476
2 1.000 0.040 11 1259904 intron variant T/C snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs4963059
rs4963059
1 11 1251628 synonymous variant C/T snv 0.32 0.29 0.700 1.000 1 2013 2013
dbSNP: rs868903
rs868903
4 0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47 0.700 1.000 1 2013 2013