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: rs11682175
rs11682175
4 0.925 0.040 2 57760458 intron variant T/C snv 0.38 0.700 1.000 5 2014 2019
dbSNP: rs11688767
rs11688767
3 0.925 0.040 2 57761059 intron variant A/T snv 0.40 0.700 1.000 1 2019 2019