SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 257
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs12788013

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/G
Orientation fwd/B
Chr-Number 11
SNP type S
Length 601
5' Near Seq 30 bp tcatggagtttaagatatagtgtattttcc
3' Near Seq 30 bp aaggtttgaactagctcttcatttctttat
Fasta Sequence AAACATGGAA GGAACACTTC AGGGGAAAGG TGGTATCTCT AAGCAAGAGA ACTGAGTGGA GTCAAGGCTG AGAGATGCAG GATAAGCAAA TGGGTAGTGA AAAGACATTC ATGAGGACAG CTAAAACAAT AAGTAATGTA AAATACAGCA TAGCAAAACT TTAACCTCCA AATCAAGCCT CTACTTGAAT CCTTTTCTGA GGGATGAATA AGGCATATGC ATCAGGGGCT GTTGCCAATG TGCATTAGCT GTTTGCAGCC TCACCTTCTT TCATGGAGTT TAAGATATAG TGTATTTTCC S AAGGTTTGAA CTAGCTCTTC ATTTCTTTAT GTTTTAAATG CACTGACCTC CCACATTCCC TTTTTAGTAA AATATTCAGA AATAATTTAA ATACATCATT GCAATGAAAA TAAATGTTTT TTATTAGGCA GAATCCAGAT GCTCAAGGCC CTTCATAATA TCCCCCAGTT TAGTAGTTGG ACTTAGGGAA CAAAGGAACC TTTAATAGAA ATTGGACAGC AAGAAAGCGA GCTTAGTGAT ACTTGTGGGC CAGGGCATTA GCCACACCAG CCACCACTTT CTGATAGGCA GCCTGCACTG
     

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