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: rs119473032
rs119473032
LZTS1
1 1.000 8 20253576 missense variant T/C snv 0.700 0
dbSNP: rs119487098
rs119487098
WWOX
1 1.000 16 78432568 missense variant T/C snv 0.700 0
dbSNP: rs121434522
rs121434522
RNF6
1 1.000 13 26215577 missense variant C/T snv 0.700 0
dbSNP: rs121434523
rs121434523
RNF6
1 1.000 13 26215158 missense variant C/T snv 0.700 0
dbSNP: rs121434524
rs121434524
RNF6
1 1.000 13 26215151 missense variant C/T snv 0.700 0
dbSNP: rs28937897
rs28937897
LZTS1
1 1.000 8 20255097 missense variant A/G snv 4.0E-06 0.700 0