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: rs11205911
rs11205911
1 1 51930640 intron variant A/G snv 0.61 0.700 1.000 1 2010 2010
dbSNP: rs12566236
rs12566236
1 1 51931271 intron variant G/T snv 0.61 0.700 1.000 1 2010 2010
dbSNP: rs6698110
rs6698110
1 1 51938469 intron variant T/C snv 0.60 0.700 1.000 1 2010 2010