ID	82
OMIM_ID	143100
Disease	HUNTINGTON DISEASE
Gene	HTT
SNP_ID	rs616617
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	G/T
Orientation	fwd/B
Chr-Number	4
SNP type	K
Length	1007
5' Near Seq 30 bp	cgtggtgagactgtaatggggtgaggcgaa
3' Near Seq 30 bp	ctgtgtgtgaagtgtcgcggcgaggcggga
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 aggcgaa K ctgtgtgtga agtgtcgcgg cgaggcggga cgaggaaggg acggggcggg actgcatggt aagggaggcg tggcgatgcg gggggcgtgg cgatgcgggg ggcgtggtga ggtaggggcg tggcgaggcc ggggcggggc acagcagggA GGCCGCCTGA ggggcggggc gagacggggg cggggcgggg cgATGCTGGG GACGGGGACA TTAGGCAGGC CGGCTGAggg gcggggcggc tgaggggcgg agcgggatag gggaggggac tggccggtga ggggtgggga ggctgggggc ggggcaggaa ggtgagaggt ggggcgaggg aggggtgggg cgcggagggg cagggcCATG GAGGGGCTCG CCCATGAAGG ACGGGGCCAT GGACGGGGCG GGGCCGTGGA GGGGGCGCCG AGCGCGGGCG CAGGCCCATG CGGAAAGGAT CCCCCGCCGA CGCCTGGAGC GGGGCGACAA CCGGCCGTGG ACTCTGAGCC GAGGTGGCCT TGGGGTTTGC CCTCCCGCCA CACTGGCCCG TGGCCAGAGC CATACTCACC CGGACAGCCC TGCGGGGAGC CAGCTGCGGG GCTCTCTGCA CGGGGAGAGG GTGGGCGAGC TCCTGCGCAG AGCGCAGAGA ATGCGCGTGG TCGGCACGAC CTGAGGACC