ID	330
OMIM_ID	107400
Disease	ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene	SERPINA1
SNP_ID	rs1540255
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/T
Orientation	fwd/B
Chr-Number	14
SNP type	Y
Length	814
5' Near Seq 30 bp	ggtaactttggatgagcggtctctccgctc
3' Near Seq 30 bp	gagcctgtttcctcatctgtcaaacgggct
Fasta Sequence	GCCTGAGGCT GGTCAAAATT GAACCTCCTC CTGCTCTGAG CAGCCTAGGG GGCAGACTAA GCAGAGGGCT GTGCAGACCC ACATAAAGAG CCTACTGTGT GCCAGGCACT TCACCCGAGG CACTTCACAA GCATGCTTGG GAATGAAACT TCCAACTCTT TGGGATGCAG GTGAAACAGT TCCTGGTTCA GAGAGGTGAA GCGGCCTGCC TGAGGCAGCA CAGCTCTTCT TTACAGATGT GCTTCCCCAC CTCTACCCTG TCTCACGGCC CCCCATGCCA GCCTGACGGT TGTGTCTGCC TCAGTCATGC TCCATTTTTC CATCGGGACC ATCAAGAGGG TGTTTGTGTC TAAGGctgac tgggtaactt tggatgagcg gtctctccgc tc Y gagcctgttt cctcatctgt caaacgggCT CTAACCCACT CTGATCTCCC AGGGCGGCAG TAAGTCTTCA GCATCAGGCA TTTTGGGGTG ACTCAGTAAA TGGTAGATCT TGCTACCAGT GGAACAGCCA CTAAGGATTC TGCAGTGAGA GCAGAGGGCC AGCTAAGTGG TACTCTCCCA GAGACTGTCT GACTCACGCC ACCCCCTCCA CCTTGGACAC AGGACGCTGT GGTTTCTGAG CCAGGTACAA TGACTCCTTT CGGTAAGTGC AGTGGAAGCT GTACACTGCC CAGGCAAAGC GTCCGGGCAG CGTAGGCGGG CGACTCAGAT CCCAGCCAGT GGACTTAGCC CCTGTTTGCT CCTCCGATAA CTGGGGTGAC CTTGGTTAAT ATTCACCAGC AGCCTCCCCC GTTGCCCCTC T