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
5 0.821 0.143 14 64227153 3 prime UTR variant G/C,T snp 0.26 0.010 1.000 1 2009 2009
dbSNP: rs1256049
rs1256049
21 0.679 0.429 14 64257333 synonymous variant C/T snp 6.7E-02 7.9E-02 0.010 < 0.001 1 2004 2004
dbSNP: rs1271572
rs1271572
15 0.715 0.357 14 64295199 intron variant A/C,T snp 1.6E-03; 0.59; 1.3E-04 0.010 < 0.001 1 2004 2004
dbSNP: rs944050
rs944050
3 0.878 0.071 14 64233327 splice region variant T/C snp 9.5E-02 9.5E-02 0.010 1.000 1 2009 2009