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: rs12564480
rs12564480
OPN3 ; WDR64
1 1.000 0.040 1 241666284 intron variant T/C snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs1841915
rs1841915
ZNF385D ; ZNF385D-AS1
1 1.000 0.040 3 21573947 intron variant G/C snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs242999
rs242999
LINC01643
1 1.000 0.040 22 34109914 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7665833
rs7665833 		1 1.000 0.040 4 130459962 intergenic variant G/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs7735612
rs7735612
SLIT3 ; LOC105377712
1 1.000 0.040 5 169082727 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019