|
|
| ID |
218 |
| OMIM_ID |
235200
|
| Disease |
HEMOCHROMATOSIS |
| Gene |
HFE
|
| SNP_ID |
rs1061482
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
6 |
| SNP
type |
M |
| Length |
734 |
| 5'
Near Seq 30 bp |
cacagtttaattttagattgtatagctata |
| 3'
Near Seq 30 bp |
acttcaatcaaataacatcatcctgtcact |
| Fasta
Sequence |
CAAACTTTAC AGTattggga ttatctggag aatgattaaa catattgagg cctgctccta
accccagaca cactgattta atgggtAATT GTTAGGTAGT TAGACATTAG CAGTTGGGAG
GGGATGACAG AAGAGAGCGG AAAGGCTGTC ACTAAGACAG CCACTGGCCC ACCTAAATTC
AGGCCCAAGA CTACCCTAAT GCCACCCTAA GGGATGGAGT TTATGATAAA GTCTGTGGCC
AAAATATCCT GGAGAAAGAG AAAGGAGGGT ACAGGTGGAA ATTCCCTAAG GTGGCACATG
CCCAACAACA CAAAAGCCTG TCTTCAAGTT CACCCCAAGT TCATCATGCC ATCATTATAA
TAGAATTTAC ATACAGTTTT GCCCCCCCAT CCCTGGGAGG CTTTTCTTAA CAAATTATAG
GTAAGACCAT GCACAGTTTA ATTTTAGATT GTATAGCTAT A
M
ACTTCAATCA AATAACATCA TCCTGTCACT CAGATACAGC CCAAACCTCA ACTCCTCCCC
ACAAACCCCA TAAAAGCACC TTGAGCTCTG TAAAGAAGTG CTGAGTTCAC TTCGCAGAAA
TAAGCCCGCT GTCCCTCAGA GTGTATTATT GTGCTTCAAT AAACTTTGCT TTAAGCTTGC
ATTTTGGTGT TAGTTTGTAG TTCTTTGCTC ACTATCACAA GAACTGAGAT TGCTGGTTCA
GAGCTCCGGC TATAATAATC TCCTCGGTTA AA
|
|
|
