Submitter | Handle | MCHAISSO | Submitter SNP ID | HG00514106824 | RefSNP(rs#) | rs5789641 | Submitted Batch ID | HG00514 | Submitted Date | Sep 15, 2017 | Publication Cited | [1] Multi-platform discovery of haplotype-resolved structural variation in human genomes | First entry to dbSNP | Sep 15 2017 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 |
| | Allele | Observed Allele | -/CTCT | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | CpG Code | N.D. |
| Validation | Validation Status | Not Validated | HWE Goodness of Fit | not applicable | Homozygote Detected | | PCR Confirmed | | In Expressed Sequence | |
| Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss3063680227|allelePos=26|len=51|taxid=9606|alleles='-/CTCT'|mol=Genomic AACCAGACTG TTTATATTCC ATGTA
N
CTCTCTCTCT GTTTATTTCT CTTTT
There is no frequency submission for ss3063680227.
No sufficient data to compute Hardy-weinberg probability for ss3063680227.
There is no individual genotype data for ss3063680227.
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