SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 246
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs35567592

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 11
SNP type Y
Length 601
5' Near Seq 30 bp cccctggaaaccatacctctactgtctgtt
3' Near Seq 30 bp ccatgagagtgacttttttatgtttcacat
Fasta Sequence GGGAGGCTGA GGCAGGAGAT TTGCTTGAAC CCAGGAGGCG GAGGTTGCAG TGAGCCAAGA TCTTGCCATT GCACTCCAGC CTGGACAACA AGAGCAAAAC TCCATCTAAA AAAAAAAAAA AATCTACTCT CTTTGCAAAT TTTAAATATA CTTACAGTAC AATTAACTAC AGTCACGATG CTGTACATTA GATATCTAGA ATTTATTCAT CCCACATAAC TGAAATTTTA TACCCTTTGA GTAATAGTTT CCTGATTCTC CCACCCCCAA CCCCTGGAAA CCATACCTCT ACTGTCTGTT Y CCATGAGAGT GACTTTTTTA TGTTTCACAT ATGAGCAAGG TTGTGTAGTA TTTGTCTTTT TGTGTCAGGC TTATTTTTCT TAGTTTTACA TCCTCCAGGT TCATCAATTC TGCCATAAAT GGCAGGATTT TCTTCTTTTT AATTTTTTTA TTTTCCTATT TTTAATTTTT TGTTTGTTAT TGAATCATCT GTGTTTCTTA TATATTTTGG ATATTAACCA AAATATTTAA GAAATATTTG GTTTGCAAAT ATGCCATTTC ATGGTTCACC TTTCATTTGT TCATTGTTTT GTTTTTTGTG
     

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