SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 391
OMIM_ID 173900
Disease POLYCYSTIC KIDNEY DISEASE
Gene

PKD1

SNP_ID

rs36032671

Organism human (Homo sapiens)
Variation Class DIP: deletion/insertion polymorphism
Alleles -/AA
Orientation fwd/
Chr-Number 16
SNP type N
Length 601
5' Near Seq 30 bp ggacggtattgcctgtcagtgaaataaata
3' Near Seq 30 bp gtcctgaccccagtgcacagacatagaggc
Fasta Sequence GCTGTGGGGC GGGTGTGTGG GCAGAGCGGT TGCCACGCCT CCCAGACTTA CTGCCCAAGC CGCCTCTGCC TTCAGATCTG CGAGGAAGCC GCCTACTCCA ACCCCAGCCT ACCTCTGGTG CACCCTCCGT CCCATAGCAA AGCCCCTGCA CAGACTCCAG CCGAGCCCAC ACCTGGCTAT GAGGTGGGCC AGCGGAAGCG CCTCATCTCC TCGGTGGAGG ACTTCACCGA GTTTGTGTGA GGCCGGGGCC CTCCCTCCTG CACTGGCCTT GGACGGTATT GCCTGTCAGT GAAATAAATA N GTCCTGACCC CAGTGCACAG ACATAGAGGC ACAGATTGCA GTCAGACAGC TCTTTTATTG ACTTTGTCTG CTTGGTGCGG GGGTTGGGGG GGTGTCGAGG CTCTAGAAGC GGCCATGCCC ACAGAAGTGG TACACAGAAG CAGGCACAGC CAGCTCCGAG GGCCTTGAGG CTGCCTGGGC CATACAGCAC ACTCGCGCGT GCGCGCGCGC ACACACACAC ACACACAGTC ACCTTCCTCC ACCCTGGGAG CCAGCCCCCA GGAGGAGTCT TTTCCTCTAA CCACCCTGGG GTCCTCTGAC
     

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