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: rs10074258
rs10074258
EFNA5
1 5 107646859 intron variant C/T snv 0.35 0.800 1.000 1 2009 2009
dbSNP: rs10781380
rs10781380
PCA3 ; PRUNE2
1 9 76793228 intron variant T/C snv 0.33 0.800 1.000 1 2009 2009
dbSNP: rs11139399
rs11139399
LOC101927502
2 9 81757826 intron variant T/C snv 0.48 0.800 1.000 1 2012 2012
dbSNP: rs11626056
rs11626056
LOC101927598
1 14 51766558 non coding transcript exon variant C/T snv 0.27 0.800 1.000 1 2009 2009
dbSNP: rs1888414
rs1888414 		1 21 20405418 intergenic variant T/C;G snv 0.800 1.000 1 2009 2009
dbSNP: rs2298948
rs2298948
GCFC2
1 2 75699439 intron variant T/C snv 0.24 0.800 1.000 1 2012 2012
dbSNP: rs2838923
rs2838923
COL18A1 ; COL18A1-AS1
1 21 45427029 intron variant A/G snv 0.42 0.800 1.000 1 2012 2012
dbSNP: rs3820201
rs3820201
SLC1A7
2 1 53115998 non coding transcript exon variant A/C;G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs6703865
rs6703865
F5
1 1 169581725 intron variant G/A snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs9315702
rs9315702
LHFPL6
1 13 39543931 intron variant C/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs959695
rs959695
VPS13B
1 8 99822954 intron variant T/C snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs12654281
rs12654281 		1 5 107704741 intron variant C/T snv 0.33 0.700 1.000 1 2009 2009