Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanCNV370v1_C_cnv10078p6 | RefSNP(rs#) | rs56371057 | Submitted Batch ID | HumanCNV370v1 | Submitted Date | Apr 14, 2009 | Publication Cited | N.D. | First entry to dbSNP | Apr 14 2009 12:00:00:000AM |
| Resource Links | 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 | INFINIUM-II | Ascertainment Samplesize | 270 | Population | N.D. |
| Allele | Observed Allele | T/C | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | SNV | 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|ss123397142|allelePos=60|len=79|taxid=9606|alleles='T/C'|mol=Genomic GACACAGCGC GCAGACCCCG GGACCCGAAG GCTAAGCTCA CATGGCTGGT AAGAAATGG
Y
GACACAGCGC GCAGACCCC
There is no frequency submission for ss123397142.
No sufficient data to compute Hardy-weinberg probability for ss123397142.
There is no individual genotype data for ss123397142.
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