ID	226
OMIM_ID	235200
Disease	HEMOCHROMATOSIS
Gene	HFE
SNP_ID	rs707889
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	fwd/B
Chr-Number	6
SNP type	Y
Length	924
5' Near Seq 30 bp	tcttctcttgtctcattgtgtttcttctga
3' Near Seq 30 bp	tgagcttgaatcacatgaaggggaacagca
Fasta Sequence	TGAAGCCCAG CAGGGCCACT AGCTGTCCCC ACCAATTACA GTCCTTGCGT AGGGTCCAAA GAAATGAATG CCAAAGAGAG CAACAGAGGA GCAAGGGAGT CACATTCCAG GACCTTCCTT CAGGGACTTT TAAAGGAAAC ATGACAGCTG AGGATCAGTT GGTTGTTTTC TGCTGTTCCC CTTCATGTGA TTCAAGCTCA Y TCAGAAGAAA CACAATGAGA CAAGAGAAGA GCCATCTCCT TCCTTCTCTA TTTATTCTAG GCATCTAAAC TACTGAATGT AGTGGTGTCT GAGATGTATC AAACGgtcag attgactgag tttgaaacct gtttctatca ctgacaaact atgagatact ctatacttca ctttcttttt tttttcattt ttttattttt atttttattt ttttgagatg gagtctcact ctgtcaccta ggctggagtg cagtggcgca aactcggctc actgcaagct ctgcctcctg ggttcatgcc attctcctgc ctcagccttc cgagtagctg ggactacagg cgtctgccac cacgcccagc taattttttg tatttttatt agagatgggg tttcaccatg ttagccagga tggtctcgat ctcctgacct cgtgatccac ccgctttggc ctcccaaagt gctgggatta caggcgtgag ccaccgtgcc cggcctactt cactttcttc atttaaaaaa gaaatgggga taatagtacc tatctcatag aattattgta agaagtgcat gcagtaatgc atgtaagtag gtgctcagaa gagtcggaca cgaagtaagt gctTTTATCA TCCTTATCAT AATTTTCATT ATCAGAACAA GGAGAGACCA GGTAGAAAAT TATTGTGATT CTTCAGGTCT GGAATACTAG AGTAGCATCC CAA