ID	251
OMIM_ID	603903
Disease	SICKLE CELL ANEMIA
Gene	HBB
SNP_ID	rs34422605
Organism	human (Homo sapiens)
Variation Class	DIP: deletion/insertion polymorphism
Alleles	-/G
Orientation	fwd/
Chr-Number	11
SNP type	N
Length	601
5' Near Seq 30 bp	ctaggtattgaataagaaaaatgaagttaa
3' Near Seq 30 bp	ggtggttgatggtaacactatgctaataac
Fasta Sequence	TTTTATGGTT TTAGGTCTTA GTTTAATTCT TTAACCCATT CAAATTTATT TTTGTTTATG GTGTAAGACA AGGGTCTGAT TTCATTTCAT TTTGAGGGTT TCACCCTCTC ATATAATAAA ATTCTTCTAT ATACCCTTCT ATCATCACTT ATTACTGATT ATATGCCTTG ATTTCAGAAT CTTGCCAACT AGATTCAGAA TTTGACTGGG AGAGAGGACA AGGACCACTT GAGACTCATA TTTTATTTCC AGAATCTAGC ATCTACCTAC CTAGGTATTG AATAAGAAAA ATGAAGTTAA N GGTGGTTGAT GGTAACACTA TGCTAATAAC TGCAGAGCCA GAAGCACCAT AAGGGACATG ATAAGGGAGC CAGCAGACCT CTGATCTCTT CCTGAATGCT AATCTTAAAC ATCCTGAGGA AGAATGGGAC TTCCATTTGG GGTGGGCCTA TGACAGGGTA ATAAGACAGT AGTGAATATC AAGCTACAAA AAGCCCCCTT TCAAATTCTT CTCAGTCCTA ACTTTTCATA CTAAGCCCAG TCCTTCCAAA GCAGACTGTG AAAGAGTGAT AGTTCCGGGA GACTAGCACT GCAGATTCCG