ID	398
OMIM_ID	173900
Disease	POLYCYSTIC KIDNEY DISEASE
Gene	PKD1
SNP_ID	rs241568
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	G/T
Orientation	fwd/B
Chr-Number	16
SNP type	K
Length	992
5' Near Seq 30 bp	gcggggcggagcgtgaaaaatagctcgtgc
3' Near Seq 30 bp	cctcggccgactctgcagtgcgacggcggt
Fasta Sequence	aaatttctta aactgtctgt gcctcagtga cctcatttaa taaagggaat aattgtagca cactttttct agagctgtga agattcaatg gaataaataA GGCAATAAAT GAATGGATGG GGAATGAAGG ATGTGGGTTT CCTCCCTCTT GTCTTTCAAT AAGCTCTCAC CATCAACCTC CCATTGCCTG Ttctctctct tccccctctc tccctctgtc tctctctcAG CCAGGAAACC TGGGGTAGGG AGGCTTGGAG CCAGCGGGTG CGTCGGGAGG CTGCGGGTAC TGACTCGGGC CGCGCACGGA GATCGCGGGA GAAGGATCCA CAACCGCGGA AGAAGGATCA GGGTGGAGCC TGTGGCTGCT GCAGGAGGAG GAACCCGCCG CCTGGCCCAC ACCACAGGAG AAGGGCGGAG CAGATGGCAC CCTGCCCACC GCTTCCCGCC CACGCACTTT AGCCTGCAGC GGGGCGGAGC GTGAAAAATA GCTCGTGC K CCTCGGCCGA CTCTGCAGTG CGACGGCGGT GCTTCCAGAC GCTCCGCCCC ACGTCGCATG CGCCCCGGGA ACGCGTGGGG CGGAGCTTCC GGAGGCCCCG CCCTGCTGCC GACCCTGTGG AGCGGAGGGT GAAGCCTCCG GATGCCAGTC CCTCATCGCT GGCCCGGTCG CGCTGTGGCG AAGGGGGCGG AGCCTGCAcc cgccccgccc cccctcgccc cgtccgcccc gcgccgcGCG GGGAGGAGGA GGAGGAGCCG CGGCGGGGCC CGCACTGCAG CGCCAGCGTC CGAGCGGGCG GCCGAGCTCC CGGAGCGGCC TGGCCCCGAG CCCCGAGCGG GCGTCGCTCA GCAGCAGGTC GCGGCCGCAG CCCCATCCAG CCCGCGCCCG CCATGCCGTC CGCGGGCCCC GCCTGAGCTG CGGCCTCCGC GCGCGGGCGG GCCTGGGGAC GGCGGGGCCA TGCGCGCGCT GCCCTAACGA TGCCGCCCGC CGC