ID	SNP51.274
OMIM_ID	agtagagacggggcttcaccatgttgggca
Disease	DIGEORGE SYNDROME
Gene	TBX1(T-box1)
SNP_ID	rs9798754
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	T-box1
Chr-Number	chromosome 22
SNP type	fwd/B
Length	Y
5' Near Seq 30 bp	1001
3' Near Seq 30 bp	gccaccatgcctggctaatttttgtatttt
Fasta Sequence	>gnl|dbSNP|rs9798754|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=127 caggatcttg ctctgtcacc caggctggag tgcagtggca tcgtgatcaa ggctcactgc agcctcaacc tcccagtctc aagcaaacct tcctcctcag tctcccgaac agctaggact acaggtgtgt gccaccacac ctggcttttt tgatgttgtt gttgttgtta gagatggggg tctcactatg ttgcccaggc tggtcacaaa ctcctgagct caagtgatcc tcccgctttt gccctccaaa gcactgggat tataggtgtg agccactgca cctggccATT GCTCCTTATT TCTTTTCTtt ctttcttttc ttcttctttt ttttttttga gacggagttt cgttctggtt gcccaggctg gagtgcaatg gcgtagtctc agctcactgc aaactccacc tcctgggctc aagcaatcct cctgcctcag cctcccaaat agctgggatt acaggcatgc gccaccatgc ctggctaatt tttgtatttt Y agtagagacg gggcttcacc atgttgggca ggctgatctc aaactcctgg gctcaaatga tccgcctgcc tcagcctccc aaagttctgg gattgtaggc atgagccacc gtgtccagcc CCTTtgaaac cccatctcta ctaaaaatat aaaagttagc tggacgtggc ggcaggtgcc tgtaatccca gctacttggg aggctgaggc aggataactg cttgaacttg ggaggtggag gttgcagtga gctgagattg caccactgca ctccagccta ggcaacaata agactccgtc tcaaacaaat aaaataaata aaaGTAGGTA AGGGGGAGAT CTGGTTCCCT GATCCGACGT CTTTCCTTGG GGTCACTGAC TGTGGGAAAG GCCTGTGCTG GGCTGAGGTG GGACCTGGTG TGGCTGTGGA GGCCGTGTCT GTGTCTGTGT CCTGTGGGCG GCTCGGCTCG TTGGGAGATG CAGTCCTGTC CTGCCCTTCC