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: rs1015164
rs1015164
CCRL2
8 0.925 3 46410189 intron variant A/C;G;T snv 0.700 1.000 2 2015 2019
dbSNP: rs10947207
rs10947207 		5 1.000 6 31393708 downstream gene variant T/C snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs13198118
rs13198118
LINC00243
4 1.000 6 30802955 intron variant T/G snv 0.17 0.700 1.000 2 2009 2010
dbSNP: rs13210132
rs13210132
MUC22
4 1.000 6 31033366 intron variant A/G snv 4.3E-02 0.700 1.000 2 2009 2010
dbSNP: rs13437082
rs13437082 		7 1.000 6 31386783 upstream gene variant C/T snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs17207190
rs17207190 		4 1.000 6 31601743 intergenic variant G/A;T snv 2.8E-02 0.700 1.000 2 2009 2010
dbSNP: rs28732144
rs28732144
LST1 ; NCR3
4 1.000 6 31588428 non coding transcript exon variant G/A snv 2.8E-02 0.700 1.000 2 2009 2010
dbSNP: rs3093661
rs3093661
TNF
4 1.000 6 31575981 intron variant G/A snv 3.5E-02 0.700 1.000 2 2009 2010
dbSNP: rs3094212
rs3094212
CDSN ; PSORS1C1
5 1.000 6 31117993 non coding transcript exon variant G/A snv 0.58 0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
CDSN ; PSORS1C1
4 1.000 6 31120157 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs3134899
rs3134899
MICB
4 1.000 6 31505509 intron variant C/T snv 0.80 0.700 1.000 2 2009 2010
dbSNP: rs3828917
rs3828917
MICB
4 1.000 6 31498140 5 prime UTR variant G/A;T snv 0.700 1.000 2 2009 2010
dbSNP: rs4711268
rs4711268 		5 1.000 6 31386727 upstream gene variant C/T snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs4711269
rs4711269 		5 1.000 6 31387042 upstream gene variant C/T snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs4959079
rs4959079 		4 1.000 6 31521102 upstream gene variant C/T snv 5.5E-02 0.700 1.000 2 2009 2010
dbSNP: rs551894425
rs551894425
CDSN ; PSORS1C1
4 1.000 6 31117993 non coding transcript exon variant G/A snv 0.700 1.000 2 2009 2010
dbSNP: rs562436976
rs562436976
CDSN ; PSORS1C1
4 1.000 6 31120157 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs720465
rs720465
TCF19 ; CCHCR1
4 1.000 6 31158000 splice region variant C/A snv 0.29 0.700 1.000 2 2009 2010
dbSNP: rs9263870
rs9263870
HCG27
4 1.000 6 31202737 non coding transcript exon variant A/G snv 0.14 0.12 0.700 1.000 2 2009 2010
dbSNP: rs9267487
rs9267487
DDX39B ; ATP6V1G2-DDX39B ; DDX39B-AS1
4 1.000 6 31543573 intron variant T/C snv 5.5E-02 0.700 1.000 2 2009 2010
dbSNP: rs9295928
rs9295928 		4 1.000 6 30855853 regulatory region variant T/C snv 0.16 0.700 1.000 2 2009 2010
dbSNP: rs9348876
rs9348876 		4 1.000 6 31607499 downstream gene variant C/G;T snv 0.700 1.000 2 2009 2010
dbSNP: rs9391701
rs9391701
MUC22
4 1.000 6 31015486 intron variant G/A snv 0.11 0.700 1.000 2 2009 2010
dbSNP: rs10039039
rs10039039
KCNIP1
5 1.000 5 170487960 intron variant C/T snv 8.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1005585
rs1005585
CBS
5 1.000 21 43056923 intron variant T/C snv 6.5E-02 0.700 1.000 1 2019 2019