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: rs6897932
rs6897932
25 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 0.900 0.909 22 2007 2018
dbSNP: rs6881706
rs6881706
2 0.925 0.120 5 35879054 3 prime UTR variant G/T snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs11567685
rs11567685
1 1.000 0.080 5 35856473 5 prime UTR variant T/C snv 0.26 0.020 < 0.001 2 2014 2017
dbSNP: rs11567686
rs11567686
1 1.000 0.080 5 35856528 5 prime UTR variant G/A snv 0.72 0.010 1.000 1 2017 2017
dbSNP: rs140673282
rs140673282
1 1.000 0.080 5 35860866 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1.000 1 2011 2011
dbSNP: rs3194051
rs3194051
4 0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 0.010 1.000 1 2017 2017
dbSNP: rs987107
rs987107
1 1.000 0.080 5 35875125 intron variant G/A snv 0.27 0.010 1.000 1 2017 2017