ID	258
OMIM_ID	300624
Disease	FRAGILE X MENTAL RETARDATION SYNDROME
Gene	FMR1
SNP_ID	rs12687886
Organism	human (Homo sapiens)
Variation Class	SNP: single nucleotide polymorphism
Alleles	C/G
Orientation	fwd/B
Chr-Number	X
SNP type	S
Length	601
5' Near Seq 30 bp	ctctatcgaacatattgcagcttgtgtcta
3' Near Seq 30 bp	aagaatgagagtggggatcgagaaagatga
Fasta Sequence	CCTGTCTGGA AGGTACTAAT AATCCAATAA GGAAAACAGA AATATAAATA AATTATTCTA GTACACTAAC CATCATAGTA GAGGTATTCA ACATTTGTTG AGTCTCTGCT ATATGCCAAG CAGTGTAATG AGGAAGCAGA GGGTATGCAC AAAGTTCTAC AAGAGCACAA AATAAGTTCT GGCAAAGGTT TGTAAAGACA TTCACAAGGG TTTTCACCAC AGTATGACTT CAGGGAGTTG GCAGTAACCT AGATGCCCGA TCAGTAGGGA TATGTATGAA TAAAATTTCT GGCATACTCG GTAGCAAACT AGGTGTACAC ACAGCAATGT GGGTATAGCT CAAAAACAGA CTGTTGAGTA AAACAGTGGG AAATAGAGAT TTACAGTCCA ATACCATCTC TGTAAATGCA AGAGGCATAA ACAAAACATT ATCTGTGTTA AATTATCAAG GATCTCTATC GAACATATTG CAGCTTGTGT CTA S AAGAATGAGA GTGGGGATCG AGAAAGATGA GGAAAAAATA ATATAAACAC TATAAAATAA TGTAAACAAG GACCCTGTAG GGACTGATAT GACAATGTGC TGAAAATTGA GGAGCAAAGT TAACTCTCTG TACCTGAGAT AAAATAACTA GCTAATAGGA ATCCAGCTGA AAACCTTAAG GTGCAGGGCC TCTATGGGGC