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: rs10817007
rs10817007
1 9 110392967 intron variant T/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs111245230
rs111245230
3 1.000 0.040 9 110407495 missense variant T/C snv 2.6E-02 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs28663144
rs28663144
2 9 110436611 intron variant A/C snv 4.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs7847526
rs7847526
1 9 110391049 intron variant T/C snv 0.15 0.700 1.000 1 2019 2019