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: rs1436109
rs1436109
NCAM1
3 1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs16855517
rs16855517
CERS6
1 2 168571553 intron variant G/A snv 1.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs409045
rs409045 		1 5 34628522 regulatory region variant C/T snv 0.66 0.700 1.000 1 2009 2009
dbSNP: rs4552930
rs4552930 		1 8 48258398 intergenic variant A/G snv 9.5E-02 0.700 1.000 1 2013 2013
dbSNP: rs4552931
rs4552931 		1 8 48258667 intergenic variant A/G snv 9.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs7205297
rs7205297
PKD1L3
1 16 71991632 intron variant G/A snv 0.77 0.700 1.000 1 2011 2011
dbSNP: rs7774046
rs7774046
KIF6 ; LOC105375047
1 6 39334656 3 prime UTR variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs7836010
rs7836010
EXT1
1 8 117849128 intron variant G/C snv 0.99 0.700 1.000 1 2011 2011