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: rs117086479
rs117086479
3 22 31993355 intron variant A/G snv 4.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs117355297
rs117355297
3 17 19020368 synonymous variant C/T snv 2.7E-02 2.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs11976181
rs11976181
3 7 142097764 intron variant T/A;C;G snv 0.64 0.700 1.000 1 2017 2017
dbSNP: rs13229622
rs13229622
3 7 142144710 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs182549
rs182549
4 2 135859184 intron variant C/T snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs9330264
rs9330264
3 1 155123274 upstream gene variant T/C snv 0.75 0.700 1.000 1 2017 2017
dbSNP: rs9825346
rs9825346
3 3 165089891 intergenic variant G/A snv 0.59 0.700 1.000 1 2017 2017