SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 239
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs10742583

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 11
SNP type R
Length 601
5' Near Seq 30 bp ttcccaattttcttattacacaaataagaa
3' Near Seq 30 bp ttgatgcactaaaagtggaagagttttgtc
Fasta Sequence CTGGCTCCTG CCCTCCCTGC TCCTGGGAGT AGATTGGCCA ACCCTAGGGT GTGGCTCCAC AGGGTGAGGT CTAAGTGATG ACAGCCGTAC CTGTCCTTGG CTCTTCTGGC ACTGGCTTAG GAGTTGGACT TCAAACCCTC AGCCCTCCCT CTAAGATATA TCTCTTGGCC CCATACCATC AGTACAAATT GCTACTAAAA ACATCCTCCT TTGCAAGTGT ATTTACGTAA TATTTGGAAT CACAGCTTGG TAAGCATATT GAAGATCGTT TTCCCAATTT TCTTATTACA CAAATAAGAA R TTGATGCACT AAAAGTGGAA GAGTTTTGTC TACCATAATT CAGCTTTGGG ATATGTAGAT GGATCTCTTC CTGCGTCTCC AGAATATGCA AAATACTTAC AGGACAGAAT GGATGAAAAC TCTACCTCAG TTCTAAGCAT ATCTTCTCCT TATTTGGATT AAAACCTTCT GGTAAGAAAA GAAAAAAAAA TATATATATA TATGTGTATA TATACACACA TACATATACA TATATATGCA TTCATTTGTT GTTGTTTTTC TTAATTTGCT CATGCATGCT AATAAATTAT GTCTAAAAAT
     

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