Submitter | Handle | SWEGEN | Submitter SNP ID | NC_000022.10:g.45225895_45225896insCT | RefSNP(rs#) | rs571105538 | Submitted Batch ID | SWEGEN | Submitted Date | May 30, 2017 | Publication Cited | N.D. | First entry to dbSNP | May 30 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 |
| Assay | Species | Homo sapiens | Molecular Type | Genomic | Method | ILLUMINA_WGS | Ascertainment Samplesize | 2000 | Population | SWEGEN |
| Allele | Observed Allele | -/CT | 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|ss3019413538|allelePos=26|len=51|taxid=9606|alleles='-/CT'|mol=Genomic GAGCTCTGGC ATTTTCTTTT TTTTC
N
CTCTCTCTCT TTTTTTTTTT TTCCC
There is no frequency submission for ss3019413538.
No sufficient data to compute Hardy-weinberg probability for ss3019413538.
There is no individual genotype data for ss3019413538.
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