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: rs10914144
rs10914144
3 1 171980610 intron variant T/C snv 0.78 0.800 1.000 4 2009 2014
dbSNP: rs2038480
rs2038480
2 1 171970501 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2180748
rs2180748
1 1 171977878 intron variant T/A;G snv 0.700 1.000 1 2014 2014
dbSNP: rs6681480
rs6681480
1 1 171925452 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs78346539
rs78346539
2 1 171966088 intron variant C/G snv 8.6E-03 0.700 1.000 1 2016 2016