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: rs11605924
rs11605924
3 1.000 0.080 11 45851540 intron variant A/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs1401419
rs1401419
2 1.000 0.040 11 45858188 intron variant T/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs2292910
rs2292910
2 1.000 0.080 11 45882062 3 prime UTR variant A/C snv 0.66 0.700 1.000 1 2012 2012