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: rs11771145
rs11771145
2 0.925 0.080 7 143413669 intron variant G/A snv 0.42 0.810 1.000 6 2011 2019
dbSNP: rs11767557
rs11767557
4 0.882 0.080 7 143412046 intron variant T/C snv 0.18 0.810 1.000 2 2011 2018
dbSNP: rs7810606
rs7810606
1 1.000 0.080 7 143411065 intron variant T/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs11763230
rs11763230
1 1.000 0.080 7 143411748 intron variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs3935067
rs3935067
1 1.000 0.080 7 143407238 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs56402156
rs56402156
1 1.000 0.080 7 143406388 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs62472729
rs62472729
1 1.000 0.080 7 143418968 intron variant G/C snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs7805776
rs7805776
1 1.000 0.080 7 143427203 intron variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs9640386
rs9640386
1 1.000 0.080 7 143435090 intron variant G/A snv 0.50 0.700 1.000 1 2018 2018