ID	491
OMIM_ID	104300
Disease	Alzheimer disease
Gene	APP
SNP_ID	rs214483
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/G
Orientation	fwd/T
Chr-Number	21
SNP type	R
Length	1313
5' Near Seq 30 bp	cttaattgcaagtctgagtaggaagttggg
3' Near Seq 30 bp	ccaacatgtgtctcccagtgctgggaaaat
Fasta Sequence	TAAGATGTGT CTTCAATTTG TATAAAATGG TGTTTTCATG TAAATAAATA CATTCTTGGA GGAGCACCAT TGTGCTGGTG TGAATGATTC CATAGTAACA ATCTTGACCA TTTACTGACG TACAGACCAG TGAGAAGTCT TCGCATGTTG GGTACCCACA CCTGTTGTGT CTTAATTGCA AGTCTGAGTA GGAAGTTGGG R CCAACATGTG TCTCCCAGTG CTGGGAAAAT ATTTCATAGA CCTAATTTAC AGTCTTTACT TGATCTAAAA CATTTTGCTG CCATATTTTG GCCCTCAAGT TTGTCCCAAA TGAGAGACAA AGGGAAAAGT TCCAGGGAAA TAAAAATTAA GACAGCTGAT TATCTGTAAA GCATGGTTTC TCATCCTGAA CGCTACTAAC ATTTTGCAGG GAATAATTCC TTGTTGAAGG GAGTTGTCCT GACCAGTGTA GGATAtttat ttattttatt tatgtttttt gagagtctcg ctctgtcacc caggctggag tgcagtggca caatctcggc tcactgcact ccagcctGGG AGACAGACGA GACTCCGTCT Caataaataa ataaataaat aaataaataa ataaaaggag ggcctggcac gaatgacatg cagggaaggc agtgagcagg tggaggtccc tgtactcgtt gtggtgcctt atctaccagg cggttgagtt gacgtctttg tggacagaat tcgattacaa aggtgtccga aagtctccag gtgggggaga gttttgtagc gggcataatt tgggttgtaa attgactgtt gtctcctgag cagtctcctg gtgagggaga gtttcactgg agctttgaaa cacatgttag acagccttgc cctgtaggga gtgtctcgtg aaggagaggt aaacaattat aattgcattt ctaaagggct aagtaggaca tgggaaactg gaaaatggag aaaagaagag aaaaaaatag taactcattc tctttttctt agaaaaatga ggatacttgg tcacatcctc acatggtgaa gaataagatg gtctcttcat ttcccttcaa cactagtccc atcgtgaggc tctgccctca tgacctaatc taatcctaac tgcctcccaa aggtcccacc tccacatccc attattgggg attagggttt caacataggg atttggggga aacacaaaca ctcagttcat agTGATATCT GACTGCGATT CCAAAGGTCT GAGGACACAT TGGCCCTGTT GTTTTTGCTG TGTTGTCCTT GGCCTCAGGT GAACATTTTA GCTTTAGATT GC