SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 107
OMIM_ID 160900
Disease DYSTROPHIA MYOTONICA
Gene

DMPK

SNP_ID

rs4803853

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 19
SNP type R
Length 401
5' Near Seq 30 bp gcgcgccggccccagcagtgggcacggggg
3' Near Seq 30 bp agagggctggtggacgggatgtccccggga
Fasta Sequence TTCCCCAACA CCGATGGGAT TTGGGAAGGA GCTCGGAATG GAGCCGCTGG AAGAGGAGAC GCGTGCGGGG AGAGGGCCCG GGCGGGTGCC TGTCCCGTCC ACACTTAGTC CCCGCGCCCC GCGGGCGCCT GAGATTGTGA GCTGGTCCCG GGAGATGTCC GAGGACCTCG GCGCGCCGGC CCCAGCAGTG GGCACGGGGG R AGAGGGCTGG TGGACGGGAT GTCCCCGGGA GAGCTGGACT TGCGCCGCCC GAGGCCCCTC ACCTCTTGCA GGGCGCGCCG CCTCCGGCCC CGGTCCGGTC GCGCTGTCGC CGGTTCTTGA ACCAGTTGCT GACCTGCGTG AGCGACAGGC CGGTGAGTGT GGCCAGGCGG CGCTTCTCGT CCGGCGTGGG GTAGCGGTTG
     

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