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: rs10265221
rs10265221
3 7 151717243 intron variant T/A;C snv 0.700 1.000 3 2016 2019
dbSNP: rs10224002
rs10224002
12 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 2 2018 2019
dbSNP: rs10254101
rs10254101
3 7 151718450 intron variant C/T snv 0.23 0.700 1.000 2 2017 2019
dbSNP: rs10224210
rs10224210
9 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs6464165
rs6464165
2 7 151716038 intron variant T/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs7805747
rs7805747
5 1.000 0.080 7 151710715 intron variant G/A snv 0.26 0.700 1.000 1 2016 2016