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: rs10918274
rs10918274
2 1.000 0.040 1 165745179 intron variant T/C snv 0.89 0.700 1.000 3 2017 2018
dbSNP: rs7555523
rs7555523
4 0.925 0.040 1 165749742 intron variant C/A snv 0.88 0.700 1.000 3 2012 2017
dbSNP: rs4657476
rs4657476
1 1 165763424 intron variant C/T snv 0.89 0.700 1.000 2 2018 2019
dbSNP: rs7518099
rs7518099
4 0.925 0.040 1 165767643 intron variant C/T snv 0.89 0.700 1.000 1 2014 2014