ID	SNP51.284
OMIM_ID	tccctcaactgatgctttcctatgtggact
Disease	DIGEORGE SYNDROME
Gene	TBX1(T-box1)
SNP_ID	rs5993829
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/C
Orientation	T-box1
Chr-Number	chromosome 22
SNP type	fwd/T
Length	M
5' Near Seq 30 bp	801
3' Near Seq 30 bp	gtggccgttgtccccatcgtccgtggcttc
Fasta Sequence	>gnl|dbSNP|rs5993829|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='A/C'|mol=Genomic|build=127 GCCAAATGAC TCGATTTCTC TACACCCCAC ATTTTACAGG TTTCAGAGCC CAAGTCAGGA GGTCAAGTGT GCATGCAAGA GGTGGCAGGG GACAGATGTG CTGCTGTTCC CAGGCCACCT GCACAGCTGG ATGGTGGAAG CAGTTCACTT AAAGGCCATG agttactcgg gaggctgagg caggaggatc acttgagcct attagttgga ggctgcagta agctatgatc atgccactgc actccagcct gggtgacaga gtgagacccc cactgtccct ggtctcttaa aagaaaaaac aaacaaacaa accaaaaaaC AAAACAGCTT ATGAGCACCT CCTACTAATT TCCTCAGCTT AGCACACCCT GTGGCCGTTG TCCCCATCGT CCGTGGCTTC M TCCCTCAACT GATGCTTTCC TATGTGGACT TCCCGGCCAG TGCTGTGGGA CCTCCCCTGT AGGGCTGGCC AGCCTCATGG GCTGGGCTAC CCGTCCCACT CAGCAGTGGC TGCCTGGCCT CCCCTCTGTC CCTCCTGCCC AGCTCCTAAT GGGCCTCCCA TAAAAGCTGA TGCGTGGGAG CCAAGCCACA GCTCGCTGAC CTGGGGAAGC TGACAGAGTG ACAGAGGGTC TCAAGGACTC TCCACCCACA AGGCGGGAAT GGGGATGCTG GCAAATCTGG TATGAAGGTT GAGACCCCGA GGAGAGGCAG GCCTGGGGGA CCGTGCAGCA GCTGTGCCCA CCTAGGACCA CAGGGCTGGT GGGGCTGGCA GCTTGGTAGA GGGCAGGTGC ACAGCAAAGT