ID	2
OMIM_ID	163950
Disease	NOONAN SYNDROME
Gene	PTPN11
SNP_ID	rs7315529
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/G
Orientation	fwd/T
Chr-Number	12
SNP type	R
Length	822
5' Near Seq 30 bp	atatgaatgaaatgggcaagcattaaaaaa
3' Near Seq 30 bp	tgaggattttggagctatacagatatgggt
Fasta Sequence	TAGATTACTC TGGCTACTAT GTGGAGATTG GATTAGGAAG TTTAGGCCTG CAGGCCTGAG ATCAGTTAAA ATGTAGCTTG TCATCTAGCT GGCCAGGATT TAGGGAGAGG GACAACTGCT TGTTAAATGG CTCTTATGTG AATTAAATTG GCATATATTA AAGGTGATCT TTGTAAGGAG CACATGATGC TGAAGCAGTT AGCACACAGT ATGAGACTCA CTTGTATATG AATGAAATGG GCAAGCATTA Aaaaa R tgaggatttt ggagctatac agatatgggt taaacttatg gctctgccat tcactagatc tgtagccttt atttatttat ttttgagaaa gagtctcacc ctgtcaccca ggctggagcg cagtggtgca gtctgggctc actgcaacct ctgcctgtcc ggttcaagca attctcccac ctcagcctcc ggagtagctg ggactacagg tgtgcgccac caagcccgac taatctttgt atttttagtt gagacggggt ctcaccatgt tggccaggct ggtcttgaac tcctgacctc aagtgatctg ctctccttgg cctcccaaag tgctgggatt acaggcgtga gccaccacgc tcagctAGAT CTGTAGCCTT CAATGAGTCA TATGCGCATC AATCAAGTAA AAGCTCTACT CTTCTCAATC TGGTCTGAGC TACCATTATT CCCAGACCAG AATACTATAG TATTCCGTAT TTTGACTGGC TTCTCTGTTT CTGGCCTTGC TCTCTTGCTC GAGCTTCACA GAGTGTCCAA AGTAATACTT CCGTACCACC CGGCCC