|
|
| ID |
221 |
| OMIM_ID |
235200
|
| Disease |
HEMOCHROMATOSIS |
| Gene |
HFE
|
| SNP_ID |
rs7762959
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
6 |
| SNP
type |
Y |
| Length |
918 |
| 5'
Near Seq 30 bp |
tgaacccaggaggcagagcttgcagtgagc |
| 3'
Near Seq 30 bp |
gagtttgcgccactgcactccagcctaggt |
| Fasta
Sequence |
AGGTAGGAGG CAAATATCTT GAAAGGGGTT GTGAAGAGGT GTTTTTTCTA ATTGGCATGA
AGGTGTCATA CAGATTTGCA AAGTTTAATG GTGCCTTCAT TTGGGATGCT ACTCTAGTAT
TCCAGACCTG AAGAATCACA ATAATTTTCT ACCTGGTCTC TCCTTGTTCT GATAATGAAA
ATTATGATAA GGATGATAAA agcacttact tcgtgtccga ctcttctgag cacctactta
catgcattac tgcatgcact tcttacaata attctatgag ataggtacta ttatccccat
ttctttttta aatgaagaaa gtgaagtagg ccgggcacgg tggctcacgc ctgtaatccc
agcactttgg gaggccaaag cgggtggatc acgaggtcag gagatcgaga ccatcctggc
taacatggtg aaaccccatc tctaataaaa atacaaaaaa ttagctgggc gtggtggcag
acgcctgtag tcccagctac tcggaaggct gaggcaggag aatggcatga acccaggagg
cagagcttgc agtgagc
Y
gagtttgcgc cactgcactc cagcctaggt gacagagtga gactccatct caaaaaaata
aaaataaaaa taaaaaaatg aaaaaaaaaa gaaagtgaag tatagagtat ctcatagttt
gtcagtgata gaaacaggtt tcaaactcag tcaatctgac CGTTTGATAC ATCTCAGACA
CCACTACATT CAGTAGTTTA GATGCCTAGA ATAAATAGAG AAGGAAGGAG ATGGCTCTTC
TCTTGTCTCA TTGTGTTTCT TCTGAGTGAG CTTGAATCAC ATGAAGGGGA ACAGCAGAAA
ACAACCAACT GATCCTCAGC TGTCATGTTT CCTTTAAAAG TCCCTGAAGG AAGGTCCTGG
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