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: rs1570271
rs1570271 		1 10 113528742 intergenic variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs17026425
rs17026425
IQCM
2 0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs17057166
rs17057166
LINC01847
1 5 159821007 intron variant C/T snv 8.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs4868304
rs4868304
LINC01942
1 5 173704454 intron variant C/T snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs6854845
rs6854845 		2 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 0.700 1.000 1 2015 2015
dbSNP: rs587779082
rs587779082
MSH2
2 2 47445584 inframe deletion CTC/- delins 0.700 0