SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 388
OMIM_ID 173900
Disease POLYCYSTIC KIDNEY DISEASE
Gene

PKD1

SNP_ID

rs28602487

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 16
SNP type R
Length 401
5' Near Seq 30 bp tcaccctcttcctggaggtgggctgggtcg
3' Near Seq 30 bp ccagtgtcacagcacggtccgggtgagccc
Fasta Sequence TGTCTGTCAG GAGTAACTGG CAAGTGCAGA CTGGGTGTGC TGGGTGGGCA CAGTGTAGTT GGTGCTTCCT GTCTGTCCGG CGCGGCCCTT GGGCCCCCAC CATCTCCCCA GTGGCAGCTG TCAGGCTGCT CAGTTGGTTA TCGCCACGCA CCACTAGGCA GCAACCAGCG TCACCCTCTT CCTGGAGGTG GGCTGGGTCG R CCAGTGTCAC AGCACGGTCC GGGTGAGCCC CAGCATGGCG GGGAGAGCTG GCATGGCCCA GGCAGGGCAG ATAGGCTGGA GGCCTCACTC CAAGGGCCCC AGGATGCTGA GGCAGCCACT GAACCAAAAC CCCGGGGCTG GTAGTCAGAG TCCAGGAGGG GCAGGAGCAT AGGGAGGTGG GCTCTGCTAG ATGCCAAGAC
     

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