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: rs11628273
rs11628273
2 14 65043160 intron variant C/T snv 0.57 0.800 1.000 2 2009 2019
dbSNP: rs11627485
rs11627485
5 14 65020976 intron variant T/C snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs11627531
rs11627531
2 14 65021078 intron variant T/C snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs12435835
rs12435835
2 14 65033191 intron variant T/G snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs4899159
rs4899159
2 14 65013877 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7148590
rs7148590
3 14 65006478 intron variant G/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs7155454
rs7155454
4 14 65035521 intron variant G/A snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs726668
rs726668
2 14 65029098 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs8006419
rs8006419
2 14 65034017 intron variant A/G snv 0.61 0.700 1.000 1 2009 2009