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: rs1051730
rs1051730
CHRNA3
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.010 1.000 1 2011 2011
dbSNP: rs17249437
rs17249437
ARG2 ; GPHN
2 1.000 0.080 14 67634170 intron variant T/C snv 0.41 0.010 1.000 1 2010 2010
dbSNP: rs3742879
rs3742879
ARG2 ; GPHN ; VTI1B
2 1.000 0.080 14 67648284 3 prime UTR variant A/C;G snv 0.21 0.010 1.000 1 2010 2010
dbSNP: rs4795405
rs4795405
LRRC3C
6 0.851 0.160 17 39932164 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs967676
rs967676
CA10
1 17 51882949 intron variant T/C snv 0.35 0.010 1.000 1 2014 2014