ID	SNP10.007
OMIM_ID	137750
Disease	GLAUCOMA
Gene	MYOC(myocilin)
SNP_ID	rs61229584
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/C
Orientation	fwd/T
Chr-Number	chromosome 1
SNP type	M
Length	821
5' Near Seq 30 bp	aattgcttgaacccgggaggcagaggtttc
3' Near Seq 30 bp	gtgagccaagatcgtgccattacactctag
Fasta Sequence	>gnl|dbSNP|rs61229584|allelePos=410|totalLen=821|taxid=9606|snpclass=1|alleles='A/C'|mol=Genomic|build=129 CTTGCCACTC CTGCAAAAAA GCATACCTAG ACTTATATTC CAGCCTCCAG AATGCCCCCT TTTCCCTAGA TCTGGCCTTG AAACAGATCT TTTGTTCCAA GCATTCCTGT ACCTTTCTGT CTTTTACCTT TAGGGTCTAT AAACCAGAGG TCAGCTGAAG GTCTTGAAAG TCAATGAACC TCATGGCCAT GTACAGGGAG GGCTCACACC TGTAATCCCA GTGCTTTGGA AGGCCGAGGT CGGCAGATCA CCTGAGGTCA GGAGTTCGAG ACTAGCCTGA CCAACATGGT GAAACCCTGT CTCTACTAAA AATACAAAAT TAGCCGGGCA TGGTGGCACA TGCCTATAAT CCCAGCTACT CAGGAGGCTG AGGTAGGAGA ATTGCTTGAA CCCGGGAGGC AGAGGTTTC M GTGAGCCAAG ATCGTGCCAT TACACTCTAG CCTGGGCAAC AAGAGTGAAA CTCTGTCTCA AAAAAAAAGA AAGAAAGTCA CTGAACTTCA GAGGAAGAGG CCAGAATTCG AGCTTTGCCA CTAACTGGTA GATGGCCATG GACAAGCTGA ATAACCTCTC TGGGCCTCAG TTTCCATATC TGCAAAAATC AGCCAGCGGT ACCGGATGCT CATTAGGTCC CTTTCCAGTT CCACATTCTT GTACTAATGT AATTTCCTGC TCATGAAAAA CATCTACTAC TAGAAAAGAA CTTCCATGTT TGGTGTTCAA TATAATGGGA TGTTGCCCTT ATTTCAAAAG TGGAGTAGCT GGAAAGATCA AGAAAAAATA TAAAATTAGG AAACACATCT AATAAATCCC CAAAGACTTG T