SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 493
OMIM_ID 104300
Disease Alzheimer disease
Gene

APP

SNP_ID

rs45599935

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles G/T
Orientation fwd/B
Chr-Number 21
SNP type K
Length 511
5' Near Seq 30 bp taaataaatacattcttggaggagcaccat
3' Near Seq 30 bp gtgctggtgtgaatgattccatagtaacaa
Fasta Sequence GGCAAGACTT TTCTTTGAAG GATGACTACA GACATTAAAT AATCGAAGTA ATTTTGGGTG GGGAGAAGAG GCAGATTCAA TTTTCTTTAA CCAGTCTGAA GTTTCATTTA TGATACAAAA GAAGATGAAA ATGGAAGTGG CAATATAAGG GGATGAGGAA GGCATGCCTG GACAAACCCT TCTTTTAAGA TGTGTCTTCA ATTTGTATAA AATGGTGTTT TCATGTAAAT AAATACATTC TTGGAGGAGC ACCAT K GTGCTGGTGT GAATGATTCC ATAGTAACAA TCTTGACCAT TTACTGACGT ACAGACCAGT GAGAAGTCTT CGCATGTTGG GTACCCACAC CTGTTGTGTC TTAATTGCAA GTCTGAGTAG GAAGTTGGGG CCAACATGTG TCTCCCAGTG CTGGGAAAAT ATTTCATAGA CCTAATTTAC AGTCTTTACT TGATCTAAAA CATTTTGCTG CCATATTTTG GCCCTCAAGT TTGTCCCAAA TGAGAGACAA AGGGA
     

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