Source: ALL
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: rs10800597
rs10800597
MIR181A1HG
1 1.000 0.040 1 198898955 non coding transcript exon variant G/A snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs10800598
rs10800598
MIR181A1HG
1 1.000 0.040 1 198900385 non coding transcript exon variant T/C snv 0.74 0.700 1.000 1 2017 2017
dbSNP: rs12406470
rs12406470
MIR181A1HG
1 1.000 0.040 1 198826991 intron variant C/T snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs60639710
rs60639710
MIR181A1HG
1 1.000 0.040 1 198898549 non coding transcript exon variant G/T snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs9660525
rs9660525
MIR181A1HG
1 1.000 0.040 1 198807802 non coding transcript exon variant C/A snv 0.38 0.700 1.000 1 2017 2017