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: rs868197660
rs868197660
GLIS3
1 1.000 0.160 9 4117797 missense variant G/A snv 0.700 0
dbSNP: rs869320723
rs869320723
GLIS3
1 1.000 0.160 9 3856143 frameshift variant -/G delins 0.700 0
dbSNP: rs879255608
rs879255608
GLIS3
1 1.000 0.160 9 4117870 missense variant G/C snv 0.700 0
dbSNP: rs879255609
rs879255609
GLIS3
1 1.000 0.160 9 4118546 frameshift variant C/- delins 0.700 0