| Submitter | | Handle | DEVINE_LAB | | Submitter SNP ID | INDEL_GP35_WGS_197493 | | RefSNP(rs#) | rs869068216 | | Submitted Batch ID | EMORY_INDEL_GP35_WGS | | Submitted Date | Jan 24, 2006 | | Publication Cited | [1] An initial map of insertion and deletion (INDEL) variation in the human genome | | First entry to dbSNP | Jan 24 2006 12:00:00:000AM |
| | Resource Links | | GenBank Accession | NT_019273
| | Submitted Gene Name | N.D | | Submitted Gene ID | N.D. | | Submitted SNP Synonyms | N.D | | Submitted linkout | N.D |
| | Assay | | Species | Homo sapiens | Molecular
Type | Genomic | | Method | METHOD_WGS | | Ascertainment Samplesize | 2 | | Population | N.D. |
| | Allele | | Observed Allele | -/TCACAG | | Ancestral Allele | N.D. | | Allele Origin | N/A | | SNP Class | DIV | | CpG Code | N.D. |
| | | Variation | | Frequency Submission | N.D. | | Genotype Summary | N.D. | | Genotype Submission | N.D. | | Haplotype | N.D. |
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>gnl|dbSNP|ss50017593|allelePos=401|len=801|taxid=9606|alleles='-/TCACAG'|mol=Genomic GGCCAAGGAG GACAGGAAAG CTCTCTGACC CACAGGTATC TGTGTTTAAT ATTCCATCCT
AGTTTCTCTT TCTCTCTCTC CTCTTTCACT TCTCTCTCTC TGTCTCTCTT TCTCTCTCTC
TCTCTCTTTC TTTTTGACAC AGGGTCTTGC TCTGTCGCCT AGGCTAGAGT ATAGCAGTGC
AATCATGGCT CACTGCAGCC TCTACCTCCT GGGCTCAGAC GATTCTTCCA CCTAAGCCTC
TTGAATAGTT GGGACTATAG GCATGCAGCA CCACAGCTGG CTAATTTTTT GTATTTATTG
TAAAGATGGG ATTCACCATA TTGTCCAGAC TGGTCTTGAA CACCTGATCT CAAGTGATCC
ACCCACCTGG GCCTCCCAAA GTGCTGTGAT TATATGGAGC
N
ACCTAGCTCC ATCCTAGTTT CTGACTCAAA CCAATATTTG TGTATACAGC TCATCCTCAG
AATTGATCTT CCATAGCCTA AACAGAGGTA TGAGACACAA GGAAAATAGA GGTTACCCAG
AAGAATGTTT AGAGCATCCT GCCATTCATC TTGAGAAGAT TCACTGTCTA CAACCAGAAT
TGAGTTGACT TTGTCTTCCT CAGATGTGAT TTTGATGTTC TTGTGAGGCG GGTTGGAGTC
AGAAGGGCCA TGGCTATTTG AATAAGTGAT GGCACATTCC TCCAGTGAGT CCTCAGGGAC
TTCCTTTTCT TCAGCCTTCT GCTCCTCCCT GATGAGCCAG GTGGGATAGA AATGACAGAA
GATTAAACAG AGAGGGATTG GATCCCAGGG AGACCTAGCT
There is no frequency submission for ss50017593.
No sufficient data to compute Hardy-weinberg probability for ss50017593.
There is no individual genotype data for ss50017593.
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