ID	76
OMIM_ID	143100
Disease	HUNTINGTON DISEASE
Gene	HTT
SNP_ID	rs386868
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	G/T
Orientation	fwd/B
Chr-Number	4
SNP type	K
Length	1022
5' Near Seq 30 bp	gggataggggaggggactggccggtgaggg
3' Near Seq 30 bp	tggggaggctgggggcggggcaggaaggtg
Fasta Sequence	ATGAATGGGG CTCTGGGCCG CAGGTAAAAG CAGAACCTGA GCGGCCGTCC ATCTTGGACC CGTCCCGGCA GCCCCCACGG CGCCTTGCGT CCCAGACGCT gcgccggcgg aggcggggcc gcgccggcgg aggcggggcc acgccggccA GCATGATTGA CAGCCCTAGC CTGCGGACTC TGCCAATGGC TGGCCAGGGA ACCAGCCCGC CCCTGCCCCC GCAGGTTCTG CCTCACACAG CAAGGCCGCT GACAGCGCAG CGCCCCACCC GGGCGAAGGC GCGGGGCTCA ACGGAGAGgg gacggggcgt ggtgagactg taatggggtg aggcgaagct gtgtgtgaag tgtcgcggcg aggcgggacg aggaagggac ggggcgggac tgcatggtaa gggaggcgtg gcgatgcggg gggcgtggcg atgcgggggg cgtggtgagg taggggcgtg gcgaggccgg ggcggggcac agcagggAGG CCGCCTGAgg ggcggggcga gacgggggcg gggcggggcg ATGCTGGGGA CGGGGACATT AGGCAGGCCG GCTGAggggc ggggcggctg aggggcggac gggatagggg aggggactgg ccggtgaggg K tggggaggct gggggcgggg caggaaggtg agaggtgggg cgagggaggg gtggggcgcg gaggggcagg gccatggagg ggctcgccca tgaaggacgg ggccatggac ggggcggggc CGTGGAGGGG GCGCCGAGCG CGGGCGCAGG CCCATGCGGA AAGGATCCCC CGCCGACGCC TGGAGCGGGG CGACAACCGG CCGTGGACTC TGAGCCGAGG TGGCCTTGGG GTTTGCCCTC CCGCCACACT GGCCCGTGGC CAGAGCCATA CTCACCCGGA CAGCCCTGCG GGGAGCCAGC TGCGGGGCTC TCTGCACGGG GAGAGGGTGG GCGAGCTCCT GCGCAGAGCG CAGAGAATGC GCGTGGTCGG CACGACCTGA GGACCCCAAG TGTGACCCCC A