ID	SNP10.020
OMIM_ID	137750
Disease	GLAUCOMA
Gene	MYOC(myocilin)
SNP_ID	rs60465115
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	fwd/B
Chr-Number	chromosome 1
SNP type	Y
Length	1001
5' Near Seq 30 bp	ccataattaaaaacctcataaataataaat
3' Near Seq 30 bp	gcagggcaatgtgcctaccttagagtaggg
Fasta Sequence	>gnl|dbSNP|rs60465115|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129 GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGCGGATCAC CTGAGGTCAG GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TTTGCTAAAA ACACAAAAGA ATTAGCTGGA TGTGGTGGCA GGTGCCTATA ATCCCAGCTT CTTGGGAGAC TGAGGCAGGA GAATTGCTTG AACCAAGGAG GGGGAGATTG CTGTGAGCCG AGACTACACT ATTGTACTCC AGCTTGGGCA ACAAGAAAGA AACTCTGTCT GAAAACTAAC TAACTAAATA AATAGGCTCC CAAAGATATG GTGTTTGAGA TTTGATTTTA GATAAGGACT GGGGATGGGT TGGGGGTCAG AGAAGGGAAG ATAAAACATG ATTGGACTGT GCTGATAACA GTTGGGCCTG AGTGATGGCT ACATTGGAGT TCATTGTAGT CTCTCTACTT TTGTGAATAT TTGAACAATT CCATAATTAA AAACCTCATA AATAATAAAT Y GCAGGGCAAT GTGCCTACCT TAGAGTAGGG TATTCAAAAT CAAATAATAT TTTAATTCCA CTAGAAGGGC TGGTTTGTGA ATAGGTGAGT CGTAATTTCA GGAATATGGA GACAGTCCTC AGCATCTTCT TAGATGTCTG AATTTCAATA ATTAAAAATT CATGAAAAAT TAGCTGGGCA TGGTGGTAAG CATCTGCAGT CCTAGGTACT TGGGAGGCTG ATGTGGGAGG ATTGCTTGAG CCCAGAAGTT CAAGGCTGCA GTGAGCTATG ATCCTGCCAC TGCACTCCAG CTTGGGTAAC AGAGCAAGGC CCGGTCTCAA GGTCTCAAAA AAAAAAAAAA AGAGACCGGG CACAGTGGCT CACACTGAAA TCCCAGCACT TTGGGAGGCC GAGGCAGGCG GATCACTTAA GGCCAGGAGT TCAAGACTAG CCTGGCCAGC GTGGTGAAAT TCCATCTTTA CTAGAAATAC AAGAATTAGC AGGGTGTGGT GGCACATGCC