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: rs1255998
rs1255998
6 0.827 0.200 14 64227153 3 prime UTR variant G/C;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1256049
rs1256049
32 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 0.010 < 0.001 1 2004 2004
dbSNP: rs1271572
rs1271572
16 0.708 0.400 14 64295199 intron variant A/C;T snv 0.010 < 0.001 1 2004 2004
dbSNP: rs3020449
rs3020449
10 0.807 0.200 14 64306674 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs944050
rs944050
5 0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 0.010 1.000 1 2009 2009