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: rs121908120
rs121908120
WNT10A
19 0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs1555316697
rs1555316697
PAX9 ; LOC105370455
2 1.000 0.080 14 36662951 missense variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs34972707
rs34972707
WNT10A
1 2 218893104 missense variant A/C snv 8.7E-04 6.1E-04 0.700 1.000 1 2015 2015
dbSNP: rs368869806
rs368869806
PTCH1
97 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs866789963
rs866789963
LRP6 ; BCL2L14
3 1.000 12 12150835 splice donor variant C/A;T snv 0.700 0
dbSNP: rs869320635
rs869320635
LRP6 ; BCL2L14
2 12 12121375 frameshift variant G/- delins 0.700 0
dbSNP: rs869320636
rs869320636
LRP6 ; BCL2L14
3 1.000 12 12138536 splice acceptor variant T/G snv 0.700 0
dbSNP: rs869320637
rs869320637
LRP6 ; BCL2L14
2 12 12203333 missense variant G/C snv 0.700 0
dbSNP: rs869320638
rs869320638
LRP6 ; BCL2L14
2 12 12179949 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs869320639
rs869320639
LRP6 ; BCL2L14
3 1.000 12 12165232 missense variant C/T snv 0.700 0
dbSNP: rs869320640
rs869320640
LRP6 ; BCL2L14
3 12 12126923 splice acceptor variant T/C snv 0.700 0