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: rs17251221
rs17251221
CASR
18 0.724 0.360 3 122274400 intron variant A/G snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs17265703
rs17265703
CSTA
4 3 122329797 intron variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs17266816
rs17266816
FAM162A
2 3 122410027 3 prime UTR variant G/A snv 7.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs17267388
rs17267388
PARP9 ; LOC105374071
2 3 122548699 intron variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs17711722
rs17711722 		2 7 65806210 downstream gene variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs2001548
rs2001548 		2 3 122313942 upstream gene variant G/A snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs2270859
rs2270859
PARP9 ; LOC105374071
3 1.000 0.040 3 122536861 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs3749203
rs3749203
CASR
2 3 122257647 intron variant C/T snv 0.45 0.700 1.000 1 2010 2010
dbSNP: rs3749208
rs3749208
CASR
2 3 122261437 intron variant C/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs3792289
rs3792289
CASR
2 3 122274753 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs3804590
rs3804590
CASR
2 3 122259226 intron variant G/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs4306808
rs4306808
FAM162A
2 3 122409619 intron variant G/C snv 0.84 0.700 1.000 1 2010 2010
dbSNP: rs4491840
rs4491840
CCDC58
2 3 122361900 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4678180
rs4678180 		2 3 122318950 downstream gene variant T/C snv 0.62 0.700 1.000 1 2010 2010
dbSNP: rs5008830
rs5008830 		2 3 122311615 intergenic variant G/A snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs6438720
rs6438720 		2 3 122298385 TF binding site variant A/C snv 0.60 0.700 1.000 1 2010 2010
dbSNP: rs6438725
rs6438725
CCDC58
2 3 122369259 intron variant T/C snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs6791616
rs6791616
FAM162A
2 3 122388388 intron variant C/T snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs6803098
rs6803098 		2 3 122321763 upstream gene variant C/T snv 0.62 0.700 1.000 1 2010 2010
dbSNP: rs7336933
rs7336933
LOC105370176
2 13 41984940 downstream gene variant G/A snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs7481584
rs7481584
CARS1
2 11 3007859 non coding transcript exon variant G/A snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2013 2013
dbSNP: rs9789994
rs9789994
KPNA1
2 3 122499004 intron variant T/A snv 0.13 0.700 1.000 1 2010 2010
dbSNP: rs9834317
rs9834317
CCDC58
2 3 122370512 intron variant G/T snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs9851884
rs9851884 		2 3 122301347 regulatory region variant A/G snv 0.66 0.700 1.000 1 2010 2010