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: rs869320627
rs869320627
OVOL2
1 1.000 0.080 20 18057973 intron variant -/GGTTCCGGCGGCCGGGGCTGCC delins 0.700 0
dbSNP: rs869320628
rs869320628
OVOL2
1 1.000 0.080 20 18058004 intron variant A/G snv 0.700 0
dbSNP: rs869320629
rs869320629
OVOL2
1 1.000 0.080 20 18057941 intron variant A/G snv 0.700 0
dbSNP: rs869320630
rs869320630
OVOL2
1 1.000 0.080 20 18057908 5 prime UTR variant A/C snv 0.700 0