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: rs11078597
rs11078597
MIR22HG ; WDR81 ; MIR22
2 17 1715069 intron variant T/C snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs11671010
rs11671010
HPN-AS1
2 19 35068570 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2012 2012
dbSNP: rs12914385
rs12914385
CHRNA3
18 0.790 0.160 15 78606381 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs16948098
rs16948098
FRMD5
2 15 43927409 intron variant G/A snv 9.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs2280401
rs2280401
RPS11 ; SNORD35B
5 19 49496752 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs2293579
rs2293579
PSMC3
2 11 47419207 intron variant G/A snv 0.35 0.30 0.700 1.000 1 2012 2012
dbSNP: rs4806073
rs4806073
HPN ; HPN-AS1
2 19 35064286 intron variant T/C snv 0.85 0.700 1.000 1 2012 2012
dbSNP: rs694419
rs694419 		2 18 62458879 regulatory region variant T/C snv 0.53 0.700 1.000 1 2012 2012