Source: BEFREE ×
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: rs2229918
rs2229918
ERCC1 ; CD3EAP
1 1.000 0.080 19 45409666 3 prime UTR variant C/G snv 4.3E-03 4.2E-03 0.010 1.000 1 2017 2017
dbSNP: rs4994
rs4994
ADRB3
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.010 1.000 1 2007 2007
dbSNP: rs759304648
rs759304648
GSN
9 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.010 1.000 1 1999 1999
dbSNP: rs774870551
rs774870551
VCL
3 0.925 0.160 10 74070712 missense variant G/A snv 1.6E-05 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs9939609
rs9939609
FTO
80 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019