ID	SNP39.010
OMIM_ID	607014
Disease	Hurler Syndrome
Gene	IDUA
SNP_ID	rs60370292
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	fwd/B
Chr-Number	chromosome 4
SNP type	Y
Length	1001
5' Near Seq 30 bp	caggtgggagcatggcttgagcccaggagt
3' Near Seq 30 bp	tgaggctgccatgaggtatgattaggccac
Fasta Sequence	>gnl|dbSNP|rs60370292|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129 GCTCTGCCTC CTGGGTTCAC GCCATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCGCCCGC CACCGCGCCC GGCTAATTTT TTTTTTTTTG AGACGGAGTT TCGCTCTGTT GCCCAGGCTG GAGTACAGTG GCATGATCTC GGCTCACTGC AAGCTCTGTC TCCCGGGTTC AAGTGATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGCACCC GCCACCACGC CCGGCTAATT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA CCATGTTAGC CAGGATGGTC TTGATCTCCT GACCTCGTGA TCCACCCACC TCGGCCTCCC AAAGTGCTGG GATTACAGGC TTGAGCCACT GCACCCGGCC GCCCCCTGCC CCCCAACCTT TAAAAAATTA AAAGTAAAAA ATTAGCTGGG TGTGGTGGTG TGTGCCTGTA TCCCAGCTAC TCAAGCGGCT CAGGTGGGAG CATGGCTTGA GCCCAGGAGT Y TGAGGCTGCC ATGAGGTATG ATTAGGCCAC TGCACCCTAT CCTAGGCCAC AGAGCAAGAG CCCGTCTCAA AAACAAACGC TGTCATTGGC CCAGCACTTT GGGAAGCTAA GGTAGGAGGA TTGCTTGAGC CCTGGAGGTC CAGGCTGCAG TGAGGTATGT TTGTAGCGCT TCACTCCAGC CTACAAGTCT TTTTTTTTTT TTTTTGAGAT GGAGTCTCGC TCTGTTGCCC AGGCTGGAGT GCAGTGGCAC AATCTCGGCT CACTGCAGCC TCTGCCTCCC GGGTTCAAGC GATTCTCCTG CCTCAGCCGC CTGAGTAGTT GGGACTACAG GCGTGTGCCA CCACGCCCGG CTAATTTTTG TATTTTTAGT AGAGACAGGG TTTCACTATG TTGGTCAGGC TAGTCTTGAA CTCCTGACCT TGTGATCCAC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGTGCC CGGCCAGTTC TGTCTCAAAA