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: rs26307
rs26307
1 1.000 0.040 5 14705556 3 prime UTR variant T/C snv 0.72 0.020 1.000 2 2005 2013
dbSNP: rs27356
rs27356
1 1.000 0.040 5 14722332 intron variant C/G;T snv 0.020 1.000 2 2005 2013
dbSNP: rs25957
rs25957
1 1.000 0.040 5 14783123 intron variant C/G snv 0.77 0.010 1.000 1 2005 2005
dbSNP: rs28006
rs28006
1 1.000 0.040 5 14781635 intron variant T/C;G snv 0.010 1.000 1 2005 2005