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: rs4823006
rs4823006
ZNRF3
5 22 29055683 3 prime UTR variant A/G snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs4858697
rs4858697
RARB
2 3 25075091 intron variant A/G snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs543874
rs543874 		11 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs564819152
rs564819152
MLLT10
1 10 21531721 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs6107848
rs6107848 		1 20 6610469 intergenic variant A/G snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs6549455
rs6549455
RYBP
1 3 72408070 intron variant A/G snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs6804842
rs6804842
RARB
3 3 25064946 intron variant A/G snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs7175517
rs7175517
MAP2K5
2 15 67785292 intron variant A/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs718314
rs718314
LOC105369705
6 0.882 0.120 12 26300350 intron variant A/G snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs741677
rs741677
VPS53
1 17 560603 intron variant A/G snv 0.46 0.52 0.700 1.000 1 2017 2017
dbSNP: rs7526762
rs7526762
TNNI3K ; FPGT-TNNI3K ; LRRC53
2 1 74527634 intron variant A/G snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs759250
rs759250 		2 2 59102018 intron variant A/G snv 0.80 0.700 1.000 1 2017 2017
dbSNP: rs7830933
rs7830933
LOC107986930
3 8 23745811 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs7864204
rs7864204
TMEM252-DT
2 9 68614263 intron variant A/G snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs7943191
rs7943191
EEF1G
1 11 62561079 intron variant A/G snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs7949030
rs7949030
GANAB
1 11 62627409 intron variant A/G snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs8066985
rs8066985 		4 17 70457204 intergenic variant A/G snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs806794
rs806794
H2AC7 ; H2BC7 ; H3C4
6 6 26200449 3 prime UTR variant A/G snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs912057
rs912057
LOC101928004
1 6 6736698 intron variant A/G snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs935111
rs935111 		2 3 42273163 intergenic variant A/G snv 0.88 0.700 1.000 1 2017 2017
dbSNP: rs987237
rs987237
TFAP2B
10 0.925 0.120 6 50835337 intron variant A/G snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs1308362
rs1308362
MRAS
2 3 138385085 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1720825
rs1720825
MRAS
2 3 138389241 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1858242
rs1858242
TAFA1
1 3 68477984 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1884897
rs1884897 		5 20 6632185 regulatory region variant A/G;T snv 0.700 1.000 1 2017 2017