Source: CURATED ×
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: rs1078643
rs1078643
TMEM238L ; TMEM220-AS1
10 0.776 0.080 17 10803924 missense variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11196170
rs11196170
TCF7L2
10 0.776 0.080 10 112962862 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11610543
rs11610543 		10 0.776 0.080 12 42740389 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1537372
rs1537372
CDKN2B-AS1
13 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs189583
rs189583 		10 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1963413
rs1963413
B9D2 ; TMEM91
10 0.776 0.080 19 41365668 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2250430
rs2250430
PLEKHG6
10 0.776 0.080 12 6312008 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2293581
rs2293581
GREM1 ; LOC100131315
10 0.776 0.080 15 32718535 5 prime UTR variant G/A;C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs34405347
rs34405347 		10 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs34548439
rs34548439
OSMR-AS1
1 1.000 0.080 5 38831029 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs35107139
rs35107139
BMP4
11 0.776 0.080 14 53952388 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs45597035
rs45597035
KLF5
10 0.776 0.080 13 73075014 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4968127
rs4968127
NXN
10 0.776 0.080 17 906403 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6066825
rs6066825
PREX1
10 0.776 0.080 20 48723580 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs61389091
rs61389091
CHRDL2
10 0.776 0.080 11 74716876 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6678517
rs6678517
LAMC1
10 0.776 0.080 1 183033504 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7121958
rs7121958
POLD3
10 0.776 0.080 11 74568967 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7708610
rs7708610 		10 0.776 0.080 5 40102341 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9470361
rs9470361 		12 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9930005
rs9930005 		10 0.776 0.080 16 80009361 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs755229494
rs755229494
APC
10 0.776 0.080 5 112761654 intron variant A/G snv 9.6E-04 0.700 1.000 1 2019 2019
dbSNP: rs145364999
rs145364999
CHD1
10 0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs35226739
rs35226739
GRM7
1 1.000 0.080 3 7428456 intron variant T/G snv 7.6E-03 0.700 1.000 1 2017 2017
dbSNP: rs116353863
rs116353863 		10 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs117079142
rs117079142
UTP23 ; LOC112268030
10 0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 0.700 1.000 1 2019 2019