ID	331
OMIM_ID	107320
Disease	ANTIPHOSPHOLIPID SYNDROME
Gene	F5
SNP_ID	rs41398055
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	A/G
Orientation	fwd/T
Chr-Number	1
SNP type	R
Length	33
5' Near Seq 30 bp	catataatattagcag
3' Near Seq 30 bp	acaatgccttttaaag
Fasta Sequence	CATATAATAT TAGCAG R ACAATGCCTT TTAAAG