ID	486
OMIM_ID	104300
Disease	Alzheimer disease
Gene	APP
SNP_ID	rs443977
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	fwd/B
Chr-Number	21
SNP type	Y
Length	951
5' Near Seq 30 bp	ttttcctactttctttaaaacttcatttcc
3' Near Seq 30 bp	tttcctctatggacccgccttgaattcttt
Fasta Sequence	GCAGCAGCTA CTCCTATAAT TCTATTTGGC AGCACTTCAG TTTTGTATAA ATTACCTATT GATTAATCCC CAGACCATTG GGAGAATACT ATCAATATAC CTCAATTTAA GAATCAAGAT TATAAGGCAT TATCTTTTCA TAATTATATA TGTATGTATA TATACATTTG GCTAGACATT TTTTTCATTA GCTTTAAAAT tgtcagaggc gtctgaacca gagcaactcc attttgaata ggggctgggt aaaataaggc tgggacctac tgggctgcat tcccagaggg ttaagtcatt ctaagtcaca ggatgagatt gtaggtctgc ataagataca ggtcataaag accttgctca taaaacaagt tgcagtaaag aagccggtca aaacccacca aaaccaagat agcaatgaga gtgacctctg gttgtcctca ctgctacact cccactagag ccatgacggt ttacaaatgc catggcaaca tcaggaagtt accctatatg gtctaccaag gggaggcatg aataattcag cccttgttta gtaaataatt aagaaataac aataaaatgg gcaaccagca gcccttaggt tcactctgcc tatggagcaa ccactcttta ttttcctact ttctttaaaa cttcatttcc Y tttcctctat ggacccgcct tgaattcttt cttgcatgag atccaagaac cctgtcttgg ggtctggatt gggacccctt tctggtaaca AAATGATCAA AGTTAAAGCT GTAGTTACTG TAACTGAGTT GGCCTTGGAA TGCCATCCCA TATAGTGCCA TGTTTGAGAG CTGGTTTTCA TTTCATTGGT GGCATTAGAA ATGTACTATT ATATTAGGGT TAATTCGCCC TGCTACCCCA ACTAGCTAGC TACCTCCCCT TGGGCCAGGC AAAATGGAAC AGTAGCTTGT