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: rs10222633
rs10222633
CASR
4 0.925 0.080 3 122258079 intron variant G/A snv 0.45 0.700 1.000 1 2010 2010
dbSNP: rs1067
rs1067
WDR5B
2 3 122414118 3 prime UTR variant G/A snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs10934578
rs10934578
CASR
4 0.925 0.080 3 122258435 intron variant G/T snv 0.30 0.700 1.000 1 2010 2010
dbSNP: rs10934582
rs10934582 		3 3 122294507 downstream gene variant G/A snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs11929034
rs11929034
PARP9 ; LOC105374071
2 3 122560202 intron variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs12107092
rs12107092
FAM162A
2 3 122405001 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs12150338
rs12150338
WDR81
2 17 1730810 synonymous variant C/G;T snv 4.0E-06; 0.12 0.800 1.000 1 2010 2010
dbSNP: rs12635478
rs12635478
CASR
2 3 122289706 3 prime UTR variant C/A snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs13083990
rs13083990 		4 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 0.700 1.000 1 2010 2010
dbSNP: rs13085498
rs13085498 		2 3 122292516 downstream gene variant C/A;T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs13085674
rs13085674 		2 3 122292504 downstream gene variant G/A snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs13095172
rs13095172
CASR
2 3 122271410 intron variant C/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs1402200
rs1402200 		2 3 122303570 intergenic variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs1472621
rs1472621 		2 3 122293879 downstream gene variant A/G snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs16832956
rs16832956 		2 3 122298661 regulatory region variant C/G;T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs16833078
rs16833078
CCDC58
2 3 122380747 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs16833080
rs16833080
CCDC58
2 3 122382060 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs16833168
rs16833168
PARP9 ; LOC105374071
2 3 122535800 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17200894
rs17200894
FAM162A
2 3 122411294 3 prime UTR variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17201246
rs17201246
KPNA1 ; LOC102723582
2 3 122426623 3 prime UTR variant C/A snv 0.13 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: 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