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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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644883 SNVs 1 of 64489 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009010706168 chr3: 6928 CE3 Intergenic A G
homozygote
MACSNP009010706172 chr3: 7011 CE3 Intergenic C T
heterozygote
MACSNP009010706173 chr3: 7019 CE3 Intergenic G T
heterozygote
MACSNP009010706207 chr3: 9420 CE3 Intergenic G A
heterozygote
MACSNP009010706208 chr3: 9612 CE3 Intergenic A G
homozygote
MACSNP009010706209 chr3: 9708 CE3 Intergenic T C
homozygote
MACSNP009010706210 chr3: 9738 CE3 Intergenic G A
heterozygote
MACSNP009010706234 chr3: 11575 CE3 Intergenic T C
homozygote
MACSNP009010706240 chr3: 11867 CE3 Intergenic G C
homozygote
MACSNP009010706242 chr3: 11937 CE3 Intergenic C T
heterozygote

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Disease-associated genes Drug-targted genes Search and download SNVs

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NCBI dbSNP Ensembl Drugbank OMIM

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