SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 255
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs7110263

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles G/T
Orientation fwd/B
Chr-Number 11
SNP type K
Length 601
5' Near Seq 30 bp aatccttttctgagggatgaataaggcata
3' Near Seq 30 bp gcatcaggggctgttgccaatgtgcattag
Fasta Sequence TTTCCTTCTT CAAGTAGACC TCTATAAGAC AACAGAGACA ACTAAGGCTG AGTGGCCAGG CGAGGAGAAA CCATCTCGCC GTAAAACATG GAAGGAACAC TTCAGGGGAA AGGTGGTATC TCTAAGCAAG AGAACTGAGT GGAGTCAAGG CTGAGAGATG CAGGATAAGC AAATGGGTAG TGAAAAGACA TTCATGAGGA CAGCTAAAAC AATAAGTAAT GTAAAATACA GCATAGCAAA ACTTTAACCT CCAAATCAAG CCTCTACTTG AATCCTTTTC TGAGGGATGA ATAAGGCATA K GCATCAGGGG CTGTTGCCAA TGTGCATTAG CTGTTTGCAG CCTCACCTTC TTTCATGGAG TTTAAGATAT AGTGTATTTT CCCAAGGTTT GAACTAGCTC TTCATTTCTT TATGTTTTAA ATGCACTGAC CTCCCACATT CCCTTTTTAG TAAAATATTC AGAAATAATT TAAATACATC ATTGCAATGA AAATAAATGT TTTTTATTAG GCAGAATCCA GATGCTCAAG GCCCTTCATA ATATCCCCCA GTTTAGTAGT TGGACTTAGG GAACAAAGGA ACCTTTAATA GAAATTGGAC
     

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