ID	47
OMIM_ID	236100
Disease	HOLOPROSENCEPHALY
Gene	SIX homeobox 3
SNP_ID	rs338069
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/T
Orientation	fwd/T
Chr-Number	2
SNP type	W
Length	958
5' Near Seq 30 bp	tgaggaattcaaaacttttttttttttttt
3' Near Seq 30 bp	aaagatcttttctgcattccgatgcagatc
Fasta Sequence	ATTATTTTTA AACTGTCTAA TTTCTCTAGG GAAAGTAACA TCGAAAGCCT AAAACAGACG CCAAAAGGCC CATAGAACAC AGAGGGCCCT CTCTGCCTCT GGCCACCACA GCCCCTAGGC CAGGCATGGG TATTTATTCT TAGGTATGTT GCTTTTAAGA AGATGTAATC AGCATCTTGA GCCGGGCCTC CCTTTGTGAG GCTTCTGTAA CTATGGAAGT GTGATTTACG CAGATTTGTC GGGGTCAGAG ACGTCTTTCC CTGAGCACTG TGTATATTTA GACAGGACTC GGTTTGGTGT TAAAAAGTGT ATATGTTGAA TGGATTCACA CACAGTAGCC AACAATGACC ACATTGTCGG CCCGTGTACA ACGCGTATTG AAACGCAGCG CCCAGACTTC AACTAATCTG CCCTCAATAA AGCTGAAATA ATTATCCTAA GCTGCCTTTC CAGAAGAAAA ATCATTGAGG AATTCAAAAC TTTTTTTTTT TTTTT W AAAGATCTTT TCTGCATTCC GATGCAGATC TGGGGGCAAG GCGCCGTGTC CACACCACTT TGGTGATCTC AATGAGGGAA GAGAGAAAGA GAGGTTGAGA GAGAATTTAA ATGGGAAACC TAACGTGACT GGGGCTGTGA GTGTCCCAGC CCCTAAACCC CGAGCTGGAG CCCTGCTTAG GCCTTGACTC CCGCAGTGCC AGGCCTCTGA GGGCCGGGGA GAAGAGCAAG CCGACAAGTG CAAGCCTCCT TGGAGGATTC CGGGCGGCAG GGAGGCCCTG GGCCCGGCGA GGGGCCAATA CTGGCTCATT TAGCCAGAGG CAGCCGTGGG GTAGCAGGTC TTCAACACGA CGACTGGGGC AGAAAAATAT TCCTCCAAAG GGAAGACCTG CCAAGCCCCA TTTCAGTGCT CTCTCCACTC CATATATATT TCCTCTCCTC CTGGCCATGA GTCCTTCTCC AC