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: rs796051887
rs796051887
1 1.000 0.040 10 6021564 missense variant C/T snv 0.800 0
dbSNP: rs796051888
rs796051888
1 1.000 0.040 10 6025968 missense variant T/G snv 0.800 0
dbSNP: rs886041032
rs886041032
1 1.000 0.040 10 6062087 splice donor variant CCTG/- delins 0.700 0
dbSNP: rs886041037
rs886041037
1 1.000 0.040 10 6024310 stop gained G/A snv 0.700 0
dbSNP: rs886041038
rs886041038
1 1.000 0.040 10 6019462 frameshift variant -/T delins 0.700 0