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: rs1562137453
rs1562137453
ADGRB3
1 6 69049307 missense variant T/C snv 0.700 0
dbSNP: rs1562308994
rs1562308994
USP45 ; TSTD3
1 6 99446205 missense variant T/C snv 0.700 0
dbSNP: rs1562391520
rs1562391520
USP45 ; TSTD3
1 6 99482871 missense variant C/T snv 0.700 0
dbSNP: rs1562456317
rs1562456317
USP45 ; TSTD3
1 6 99508705 missense variant A/C snv 0.700 0
dbSNP: rs1563293555
rs1563293555
HOOK3
1 8 42930130 missense variant T/G snv 0.700 0
dbSNP: rs1563765580
rs1563765580
RUNX1T1
1 8 92017274 frameshift variant -/A ins 0.700 0
dbSNP: rs1564726619
rs1564726619
HKDC1 ; LOC101928994
1 10 69232838 missense variant G/T snv 0.700 0
dbSNP: rs1565117343
rs1565117343
OSBP
1 11 59594048 stop gained G/A snv 0.700 0
dbSNP: rs1565272952
rs1565272952
PIK3C2A
1 11 17145862 splice donor variant C/A snv 0.700 0
dbSNP: rs1565798439
rs1565798439
ZFC3H1
1 12 71610513 missense variant A/G snv 0.700 0
dbSNP: rs1566529937
rs1566529937
RASA3
1 13 114052075 missense variant A/G snv 0.700 0
dbSNP: rs1566615893
rs1566615893
RNF31
1 14 24155442 missense variant A/G snv 0.700 0
dbSNP: rs1567280099
rs1567280099
ANKS3
1 16 4697038 frameshift variant -/G delins 0.700 0
dbSNP: rs1567547614
rs1567547614
FBRS
1 16 30668622 missense variant G/A snv 0.700 0
dbSNP: rs1567858976
rs1567858976
PSMD11
1 17 32477518 splice region variant CAGA/- delins 0.700 0
dbSNP: rs1567966432
rs1567966432
GREB1L ; LOC101927521
1 18 21383629 missense variant T/G snv 0.700 0
dbSNP: rs1568105562
rs1568105562
FZD2
1 17 44559091 missense variant T/G snv 0.700 0
dbSNP: rs1568162263
rs1568162263
MED24
1 17 40029767 missense variant G/C snv 0.700 0
dbSNP: rs1568383758
rs1568383758
BRD4
1 19 15255488 missense variant C/A snv 0.700 0
dbSNP: rs1569148952
rs1569148952
H2AP ; SYTL5
1 X 37991160 frameshift variant TG/- del 0.700 0
dbSNP: rs1569197778
rs1569197778
USP51 ; LOC101928692
1 X 55488927 stop gained G/A snv 0.700 0
dbSNP: rs1569405174
rs1569405174
AMMECR1 ; LOC105373312
1 X 110317618 frameshift variant G/- delins 0.700 0
dbSNP: rs193922466
rs193922466
SHOX
1 Y 634687 missense variant A/G snv 0.700 0
dbSNP: rs200034765
rs200034765
HKDC1
1 10 69247416 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs201306926
rs201306926
CLGN
1 4 140399004 missense variant T/C snv 3.6E-05 7.0E-06 0.700 0