Gene: RCL1 ×
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: rs10758656
rs10758656
RCL1
7 9 4852599 intron variant A/G snv 0.19 0.800 1.000 2 2009 2019
dbSNP: rs10758658
rs10758658
RCL1
4 9 4856877 intron variant G/A snv 0.15 0.700 1.000 2 2017 2018
dbSNP: rs1053872
rs1053872
RCL1
4 0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10758657
rs10758657
RCL1
2 9 4853751 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10815094
rs10815094
RCL1
2 9 4845520 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10815095
rs10815095
RCL1 ; MIR101-2
4 9 4848297 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs10815098
rs10815098
RCL1
2 9 4865338 intron variant C/T snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs10974808
rs10974808
RCL1
3 9 4840380 intron variant A/G snv 9.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs10974815
rs10974815
RCL1
2 9 4854253 intron variant C/T snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs13284787
rs13284787
RCL1
2 9 4811553 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs13300663
rs13300663
RCL1
3 9 4814948 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2236496
rs2236496
RCL1
5 9 4844265 intron variant T/C snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs2236497
rs2236497
RCL1
2 9 4844704 intron variant T/C snv 0.22 0.19 0.700 1.000 1 2009 2009
dbSNP: rs4740804
rs4740804
RCL1
2 9 4861479 intron variant C/T snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs7853365
rs7853365
RCL1
3 9 4855858 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7868737
rs7868737
RCL1
2 9 4843672 intron variant C/G snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs7874244
rs7874244
RCL1
1 9 4847570 intron variant T/A;C snv 0.700 1.000 1 2016 2016