SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 394
OMIM_ID 173900
Disease POLYCYSTIC KIDNEY DISEASE
Gene

PKD1

SNP_ID

rs2855372

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles G/T
Orientation fwd/B
Chr-Number 16
SNP type K
Length 435
5' Near Seq 30 bp ttccggaggccccgccctgctgccgaccct
3' Near Seq 30 bp tggagcggagggtgaagcctccggatgcca
Fasta Sequence GGTGCGTCGG GAGGCTGCGG GTACTGACTC GGGTCCGCGC ACGGAGATCG CGGGAGAAGG ATCCACACCG CGGAAGAAGG ATCAGGGTGG AGCCTGTGGC TGCTGCAGGA GGAGGAACCC GCCGCCTGGC CCACACCACA GGAGAAGGGC GGAGCCAGAA TGGCACCCTG CCCACCGCTT CCCGCCCACG CACTTTAGCC TGCAGCGGGG CGGAGCGTGA AAAATAGCTC GTGCGCCTCG GCCGACTCTG CAGTGCGACG GGCGGAGGTT CCAGACGTTC CGCCCCACGT CGCATGCGCC CCGGGAACGC GTGGGGCGGA GCTTCCGGAG GCCCCGCCCT GCTGCCGACC CT K TGGAGCGGAG GGTGAAGCCT CCGGATGCCA GTCCCTCATC GCTGGCCCGG TCGCGCTGTG GCGAAGGGGG CGGAGCTTGC AA
     

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