Submitter | Handle | MCHAISSO | Submitter SNP ID | NA19240782314 | RefSNP(rs#) | rs5874297 | Submitted Batch ID | NA19240 | 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 | -/AA | 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. |
|
>gnl|dbSNP|ss3066064680|allelePos=26|len=51|taxid=9606|alleles='-/AA'|mol=Genomic CTATTGCTAC AAATTTGCCA CCAAG
N
AAAAAAAAAA AAAGTTCCAG AAGGG
There is no frequency submission for ss3066064680.
No sufficient data to compute Hardy-weinberg probability for ss3066064680.
There is no individual genotype data for ss3066064680.
|