SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 238
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs16911894

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/G
Orientation fwd/
Chr-Number 11
SNP type S
Length 331
5' Near Seq 30 bp caayttcttatttgtgtaataagaaaattg
3' Near Seq 30 bp gaaaacgatcttcaatatgcttaccaagct
Fasta Sequence GGAGACGCAG GAAGAGATCC ATCTACATAT CCCAAAGCTG AATTATGGTA GACAAAACTC TTCCACTTTT AGTGCATCAA YTTCTTATTT GTGTAATAAG AAAATTG S GAAAACGATC TTCAATATGC TTACCAAGCT GTGATTCCAA ATATTACGTA AATACACTTG CAAAGGAGGA TGTTTTTAGT AGCAATTTGT ACTGATGGTA TGGGGCCAAG AGATATATCT TAGAGGGAGG GCTGAGGGTT TGAAGTCCAA CTCCTAAGCC AGTGCCAGAA GAGCCAAGGA CAGGTACGGC TGTCATCACT TAGACCTCAC CCTGTGGAGC CAC
     

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