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: rs3825942
rs3825942
15 0.716 0.320 15 73927241 missense variant G/A;C;T snv 0.18; 4.5E-06 0.900 0.955 44 2007 2019
dbSNP: rs2165241
rs2165241
15 0.716 0.360 15 73929861 intron variant T/C snv 0.60 0.800 1.000 23 2008 2019
dbSNP: rs11634339
rs11634339
1 1.000 0.040 15 73913466 intron variant T/C snv 0.36 0.700 1.000 1 2014 2014
dbSNP: rs1550437
rs1550437
1 1.000 0.040 15 73928957 intron variant C/T snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs1048661
rs1048661
14 0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 0.100 0.892 37 2008 2019
dbSNP: rs41435250
rs41435250
2 0.925 0.040 15 73927743 synonymous variant G/T snv 6.1E-02 3.7E-02 0.020 1.000 2 2013 2019
dbSNP: rs16958477
rs16958477
2 0.925 0.040 15 73926125 5 prime UTR variant A/C snv 0.33 0.010 1.000 1 2015 2015