ID	389
OMIM_ID	173900
Disease	POLYCYSTIC KIDNEY DISEASE
Gene	PKD1
SNP_ID	rs36099770
Organism	human (Homo sapiens)
Variation Class	DIP: deletion/insertion polymorphism
Alleles	-/G
Orientation	fwd/
Chr-Number	16
SNP type	N
Length	601
5' Near Seq 30 bp	ggtgtggtggtgccgagatggggtgcacgg
3' Near Seq 30 bp	ctcacttcatggctgggcagacggattcgg
Fasta Sequence	CACCCTCTTC CTGGAGGTGG GCTGGGTCGG CCAGTGTCAC AGCACGGTCC GGGTGAGCCC CAGCATGGCG GGGAGAGCTG GCATGGCCCA GGCAGGGCAG ATAGGCTGGA GGCCTCACTC CAAGGGCCCC AGGATGCTGA GGCAGCCACT GAACCAAAAC CCCGGGGCTG GTAGTCAGAG TCCAGGAGGG GCAGGAGCAT AGGGAGGTGG GCTCTGCTAG ATGCCAAGAC AACCAGTTGG GGGGGGGGGG GCACCTGGGC GGCTGAGGAG GGTGTGGTGG TGCCGAGATG GGGTGCACGG N CTCACTTCAT GGCTGGGCAG ACGGATTCGG ACGTGTGGCT GCAGACACCC TGGGGGCCCC AGTGAGTGGA GGTGCCCCAG CAATTAGAGG TGTCTTGCCT GTGGCTGCAG CATATGTGGG TGCTGCGCCC AGATGTGGAG GGGGCTTGGC CTGGGGGAGG CCAGACAAAC ACAGCCCCGC TGCCAGAGGG GAAAGTTCAG GGGCAGATGC TGCCCATGGA GCTGACAGGT GTCTAGCAGT GCAACCAGGC AGTAGCCGAG ATCAGCCTTC AGCACACGCT GTGTGCGGGG ATGACCCTTT