Filter SNPs Using Feature Selection

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285821 SNPs 1 of 28583 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002062033227 chr14: 3686 CR2 Intergenic A G
homozygote
MACSNP002062033230 chr14: 3801 CR2 Intergenic T C
homozygote
MACSNP002062033250 chr14: 4605 CR2 ENSMMUG00000011501: Intron
G A
heterozygote
MACSNP002062033274 chr14: 5372 CR2 ENSMMUG00000011501: Intron
A T
homozygote
MACSNP002062033275 chr14: 5401 CR2 ENSMMUG00000011501: Intron
T C
homozygote
MACSNP002062033280 chr14: 5481 CR2 ENSMMUG00000011501: Intron
G T
homozygote
MACSNP002062033281 chr14: 5507 CR2 ENSMMUG00000011501: Intron
T C
homozygote
MACSNP002062033293 chr14: 5917 CR2 Intergenic T C
homozygote
MACSNP002062033304 chr14: 6266 CR2 Intergenic A C
homozygote
MACSNP002062033339 chr14: 7844 CR2 ENSMMUG00000011502: 5'UTR
G A
heterozygote