Gene: GC ×
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: rs2282679
rs2282679
GC
38 0.645 0.480 4 71742666 intron variant T/G snv 0.21 0.800 1.000 4 2010 2018
dbSNP: rs4588
rs4588
GC
53 0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 0.700 1.000 2 2017 2018
dbSNP: rs1155563
rs1155563
GC
4 0.925 0.080 4 71777771 intron variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs3755967
rs3755967
GC
6 0.925 0.080 4 71743681 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7041
rs7041
GC
64 0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs843005
rs843005
GC
2 4 71750610 intron variant C/A;T snv 0.700 1.000 1 2018 2018