ID	SNP51.264
OMIM_ID	tttttttttttgttttttttttttgagatg
Disease	DIGEORGE SYNDROME
Gene	TBX1(T-box1)
SNP_ID	rs12168076
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	G/T
Orientation	T-box1
Chr-Number	chromosome 22
SNP type	fwd/B
Length	K
5' Near Seq 30 bp	1001
3' Near Seq 30 bp	ggttcagatttctccacacacttgttttct
Fasta Sequence	>gnl|dbSNP|rs12168076|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=120 cctcattccc ctcccctggc agccagcatt ctactctctg tctctgtgaa tctgactact ctaggcgcct catgtaagtg gaatcacaca gcatttgtct ttttgtggct ggcttagttc actgagtgta aggacctcaa ggttcatccg tgttctagcc tgtgtcggaa ctccctgcct ttataaggct gaacactatt ctgttgtatg tctgtaccac gttttgttga ttcattcttc tgtcaatgga cacttgggtt gctcccacct gttggctgct gtgagtaatg ccgctatgaa cgtgggtata gaaatatctt tgcagccctg ctttcagttc tcttgggtat tctgccacaa gaggaactgc tggctcatat ggtaattcta tgtccaggat tttgagaaat gaccacactg ttttccatag ctgctactcc atttttacat tcccaccaat agcgcacaag ggttcagatt tctccacaca cttgttttct K tttttttttt tgtttttttt ttttgagatg gagtctcgct ccgtcgccca ggctggagtg cagtggcgcg atctcggctc actgcaagct ctgcctcctg ggttcatgcc attctcctgc ctcagcctcc cgagtagcta ggactacagg tgcccgccac cacgcccagc taattttttg tagttttagt agagacgggg ttttaccatg ttagccagga tggtctcgat ctcctgacct cgtgatccac ccgcctcagc ctcccaaagt gctgggatta caggcgtgag ccactgcacc cggccctgtt ttgtttttat ttttggtgta cccatcctca tgggtgtaag gcagtatctg tctcattata gttctgactt gcatttcccc agaggatagt gatgctgtgc ctgctggcta ctcatacatc ttctttggag atatgtctac ttaagtcatt tgtctatttt ttTTTAATTT TTAATTTTTA GAGACAGGGT