ID	SNP39.144
OMIM_ID	607014
Disease	Hurler Syndrome
Gene	IDUA
SNP_ID	rs1814546
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/G
Orientation	fwd/T
Chr-Number	chromosome 4
SNP type	R
Length	850
5' Near Seq 30 bp	gtttccatttcctgacctcgtgatccgccc
3' Near Seq 30 bp	ccttggcttccagagcatttttcaaggatc
Fasta Sequence	>gnl|dbSNP|rs1814546|allelePos=501|totalLen=850|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129 CAGCCAGCAG GAAGACATCC AGGCAGCAGA TGGCATCGCC AGTGCAAAGG CTCTGGAACA GGAATGCACA CATGACAATC AGGCAGCAGG GAGGCAGCTG GTGGGCCTGA GACAGAATAA GGGTGGATAT CATGGGATAT GAGGCTCCAT GGGGCTCTGG AAGTGACTGC TTTGAGGATG GGACCCTGAC CCAGAGCGAA ACAAGGATCC CTTTCAAGGT TCTGAGCTGA GCAGTGCCAG GGCAtttttc ttttttcttt tttttttttt tgagacagag tctcactctg ttgcccagcc tggggtgcag tggcgcgatc tcggctcact gcaagctccc cctcccgggt tcacaccatt ctcctgcctc agcctcctga gtagctggga ctacaggcgc ccgccaccac gcccggctaa tttttttgta tttttagtag agacggagtt tcaccatgtt agccaggatg gtttccattt cctgacctcg tgatccgccc R ccttggcttc cAGAGCATTT TTCAAGGATC CCTCTGGCAG CTCACTGGAG TCAGGGTGGG AGCTGGAAGA CTGGCTGGGG GCCATGGGGG TTGCCCAGAG AGGTATGGTG CCCAGACTGG GTGGTGGCTG TGCAGGCTGT GAGCAGAGGG ACTGATGAGG TTTGAGGTGA GCTGGGGGGT GAGGTGGGGG GTCGGGGGGT CGTACAGGGC AACTGTGGAT TTCAGCTTGG GCAGCTAGGC GGGTGGATGA GCTTGGAGTG AGACTGGTCT CGGTTTTGGC CATGTGGAGT TGGACATCTG AGGGTGAACT GAGTGAGGAG ATTGGTGTGC AAGGGTCTGG AGTTGTGAG