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: rs117298325
rs117298325
1 1.000 0.080 6 31312441 intron variant T/C snv 9.6E-03 0.700 1.000 1 2018 2018
dbSNP: rs12111032
rs12111032
1 1.000 0.080 6 31274414 intron variant A/G snv 0.23 0.700 1.000 1 2015 2015