ID	454
OMIM_ID	120435
Disease	LYNCH SYNDROME
Gene	MSH2
SNP_ID	rs12612908
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	fwd/B
Chr-Number	2
SNP type	Y
Length	1001
5' Near Seq 30 bp	ggctgggcacaggaatatgtttaaatcccc
3' Near Seq 30 bp	cccacctccccagggtgattctgctgctga
Fasta Sequence	cccaggaagt ggaggttgca gtgagctgag attgtgccat tgcactccag cctgggcaac aagagcgaaa ctccatctca aaaaacaaac aaacaaacaa acaaaaaaca aaaccaaaaa aaaaaaaaaT GATTCCAagc tgggcatggt ggctcacacc tgtaatccca gcactttggg aggccgaggc gggcagaaca ggaggtcaag agatcgagac cagaccatcc tggccaacac agtgaaaccc cgtctctcct aaaaatacca aaattagctg ggggtggtgg tgcacacctg tagtcatagc tacttgggaa gctgaggcag gaggatcgcc tgaacccggg aggcagtgag ccgagattgc gccactgcac tccagtgtgg tgacagagcc agacttcctc tcaaaaaaac aaacaaaGGT TCCAAGGCTC TACTCCAGAA ATTAAGACCC ATTATGTGTG GGCTGGGCAC AGGAATATGT TTAAATCCCC Y CCCACCTCCC CAGGGTGATT CTGCTGCTGA ATTAGGTTTT GGAACCACTT CCATGGGGAA AGGGTAAACT AAACTGGAGA ATGCAAAAAC Cttttttttt tttttttttt tttttgagac agagtctcac cctgttgccc aggctggagt gcaatggcgc gacctcggct cactgcaacc tccacctccc aggttcaagg gattctcctg cctcagcctc ccaagtagct gggattacag gtgcccacca ctacacccgg ctaattttgt gtgtgttttt agtagagacg gaggttcacc atgttagtca ggctggtctc gaactcctga cctcaggtga tctgcccgcc tcggcctccc aaagtgctgg gattacaggc gtgagccacc gcgcccggcc AGCAAAAACC TTTTCTAAGA GTTAATTTTG CAGGATGGAT CCTGAGCTCC TTCAGGTGTT TGATAACATT TTATTTATTT TTTGAGACAG AGTCTCGCTC