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: rs6750228
rs6750228
NRXN1 ; LOC730100
1 2 51084986 intron variant T/A snv 6.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs6768627
rs6768627
MYL3
1 3 46853886 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs702634
rs702634
ARL15
3 1.000 0.080 5 53975590 intron variant G/A snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs7654754
rs7654754
SHROOM3
1 4 76488642 intron variant G/A snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs7670121
rs7670121
NR3C2
1 4 148207444 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs7731168
rs7731168
CWC27
1 5 65000644 intron variant G/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs784257
rs784257
LOC105372130
4 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs8035855
rs8035855
MAPKBP1
1 15 41785763 intron variant G/A snv 0.59 0.700 1.000 1 2018 2018
dbSNP: rs838142
rs838142
FUT1 ; IZUMO1
1 19 48748894 3 prime UTR variant A/G snv 0.39 0.700 1.000 1 2018 2018