ID	446
OMIM_ID	219700
Disease	CYSTIC FIBROSIS
Gene	TGFB1
SNP_ID	rs10406316
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	G/T
Orientation	fwd/B
Chr-Number	19
SNP type	K
Length	701
5' Near Seq 30 bp	gagagaattcacaagcaggaccatagcaga
3' Near Seq 30 bp	gggaagaaatggagacagcagagggagacc
Fasta Sequence	GGCCCCAGGT CCCTGGCACC CAGACCCAGT GCTGCCAACA GCTCTCATGC CCACAGGCAA AGGAACCGCA GCACTCATAC TGTCCTTCCT CCCAGGACAA TCACTGGGTG TGGGGAAGTG AAACCTAGGA GAAAGAGCAG AAACTGAGAG GCAGGAGAAA GAGGAAGCAG GAGAGAATTC ACAAGCAGGA CCATAGCAGA K GGGAAGAAAT GGAGACAGCA GAGGGAGACC CACCTGTGGC TGCTGCCATT TCTTGCCTGG ACAGCTGGTC TGTCTGTGCT CACCCTCACC CTGACACTTC TGTCCACTCC CAACCATGAG CAAGACGGCG GACCCTCTGA GCGCCTAGGT CAAACCCTGC CATGGCTCCT GTCTTCCTTG AGTGCAAGtt cttttttttt ttttttttga gatggagtct cactctgttg cccaggctgg agtgcagtgg tgcgacttta gctcactgca acctctgcct cccctgttca tgcgattctc ctgcctcagg cccctgagta gctgggatac aggtgtgcac cacaatgcca gactaatttt tttttgtatt tttTAttttt atttatttat ttgagatgga gtctcactct gtctcccagg ctggagtgaa gtggcgtgat ctcggctcac tgcaacctcc acctcccagg ttcaagcgat tctcctgcct cagcctcctg