ID	SNP39.117
OMIM_ID	607014
Disease	Hurler Syndrome
Gene	IDUA
SNP_ID	rs4323045
Organism	human (Homo sapiens)
Variation Class	MIXED: cluster contains submissions from 2 or more alleleic classes
Alleles	-/C/G
Orientation	fwd/T
Chr-Number	chromosome 4
SNP type	N
Length	801
5' Near Seq 30 bp	gcaagccggtgctcacggccatggggcttg
3' Near Seq 30 bp	gctgctgggtgagccggggccgctggggtg
Fasta Sequence	>gnl|dbSNP|rs4323045|allelePos=401|totalLen=801|taxid=9606|snpclass=7|alleles='-/C/G'|mol=Genomic|build=114 ATTTACAACG ACGAGGCGGA CCCGCTGGTG GGCTGGTCCC TGCCACAGCC GTGGAGGGCG GACGTGACCT ACGCGGCCAT GGTGGTGAAG GTGGGCCGGC CCAACGCCCT GCGCGCCCCC CGGCCACCTT CCTCCCGAGA CGGGACAGGC GAGCGGTGGC CGCGCCACCC GGTCCCAGCT GCCCTGGACA CCCGCAGGTC ATCGCGCAGC ATCAGAACCT GCTACTGGCC AACACCACCT CCGCCTTCCC CTACGCGCTC CTGAGCAACG ACAATGCCTT CCTGAGCTAC CAGCCCGCAC CCTCTTCGCG CANGGACTCA CGCGCGCTTC CAGGTCAACA ACACCCGCCC GCGCACGTGC AGCTGTTGCG CAAGCCGGTG CTCACGGCCA TGGGGCTTGG N GCTGCTGGGT GAGCCGGGGC CGCTGGGGTG GCCGCCAGGC CCTCCAGGCT GGGGAGCGGC TCCTGCGAAG GCCCCGCTGC GGGGAGCGCA CTTCCTCCAG CCGCGCGCTT CCCGGGGTCG GCCTCCGCGT GGCGGGGCCT GGGGACTCCT TCACCAAGGG GAGGGGGAGC GAGTGGTGGG AGGCCCGGCC CTGGGTCGGG GGGCGGCTGG GCAACGACCC CACGCGGCGA CGGCCCCCCC CCGCCCCGCA GATGAGGAGC AGCTCTGGGC CGAAGTGTCG CAGGCCGGGA CCGTCCTGGA CAGCAACCAC ACGGTGGGCG TCCTGGCCAG CGCCCACCGC CCCCAGGGCC CGGCCGACGC CTGGCGCGCC GCGGTGCTGA TCTACGCGAG CGACGACACC