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: rs13037010
rs13037010
1 20 52369760 intron variant G/A snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs16996700
rs16996700
3 20 52365406 intron variant T/C snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs2904155
rs2904155
1 20 52346704 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6021889
rs6021889
1 20 52366331 intron variant A/G snv 0.34 0.700 1.000 1 2019 2019