SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 387
OMIM_ID 173900
Disease POLYCYSTIC KIDNEY DISEASE
Gene

PKD1

SNP_ID

rs28721933

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/G
Orientation fwd/
Chr-Number 16
SNP type S
Length 401
5' Near Seq 30 bp aggagtaactggcaagtgcagactgggtgt
3' Near Seq 30 bp ctgggtgggcacagtgtagttggtgcttcc
Fasta Sequence CCACTGCTGT GTCCCGGGTT GGTGGCAGGT CCTCCTCCCT GAGCTTCGGT CACGAGGAGC AGGAGGAGAG GCCGCAGTGC TCAGGGCCCC GTGGGCACGA GCTTCACCCC GAGCCTGCGT TGTGTCCTCT GTGCCCTGAA GCCTGTGGCG CCTGCTGCTG AGTGTCTGTC AGGAGTAACT GGCAAGTGCA GACTGGGTGT S CTGGGTGGGC ACAGTGTAGT TGGTGCTTCC TGTCTGTCCG GCGCGGCCCT TGGGCCCCCA CCATCTCCCC AGTGGCAGCT GTCAGGCTGC TCAGTTGGTT ATCGCCACGC ACCACTAGGC AGCAACCAGC GTCACCCTCT TCCTGGAGGT GGGCTGGGTC GGCCAGTGTC ACAGCACGGT CCGGGTGAGC CCCAGCATGG
     

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