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: rs17187619
rs17187619
HRH4
1 1.000 18 24469616 intron variant T/C snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs4800573
rs4800573
HRH4
1 1.000 18 24479706 3 prime UTR variant G/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs487202
rs487202 		1 1.000 18 24482852 downstream gene variant G/C;T snv 0.010 1.000 1 2012 2012
dbSNP: rs527790
rs527790 		1 1.000 18 24480951 downstream gene variant C/T snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs574913
rs574913 		1 1.000 18 24483244 downstream gene variant G/A snv 0.91 0.010 1.000 1 2012 2012