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: rs879255245
rs879255245
GRHL3
1 1.000 0.120 1 24342238 missense variant C/T snv 4.0E-06 0.800 1.000 1 2014 2014
dbSNP: rs752673677
rs752673677
GRHL3
1 1.000 0.120 1 24338044 missense variant G/A snv 2.0E-05 7.0E-06 0.800 0
dbSNP: rs1553172687
rs1553172687
GRHL3
1 1.000 0.120 1 24338050 stop gained G/A snv 0.700 0
dbSNP: rs879255243
rs879255243
GRHL3
1 1.000 0.120 1 24347483 frameshift variant GGAG/- delins 0.700 0
dbSNP: rs879255244
rs879255244
GRHL3
1 1.000 0.120 1 24343026 splice donor variant G/T snv 0.700 0
dbSNP: rs879255573
rs879255573
GRHL3
1 1.000 0.120 1 24339684 frameshift variant -/GT delins 0.700 0
dbSNP: rs946439477
rs946439477
GRHL3
1 1.000 0.120 1 24347483 missense variant G/A snv 4.0E-06 7.0E-06 0.700 0