| Submitter | | Handle | EGCUT_WGS | | Submitter SNP ID | VAR22258880 | | RefSNP(rs#) | clustering in process | | Submitted Batch ID | E22 | | Submitted Date | Aug 28, 2018 | | Publication Cited | [1] Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records | | First entry to dbSNP | Aug 28 2018 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 | PCR_FREE_WGS | | Ascertainment Samplesize | 2240 | | Population | EGCUT_WGS |
| | Allele | | Observed Allele | G/A | | Ancestral Allele | N.D. | | Allele Origin | N/A | | SNP Class | SNV | | 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|ss3676520632|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic CTTCAAATTG AGTTTTGAAT AGGGA
R
TCATAAAAAA AGAGATAAAT GTTTA
There is no frequency submission for ss3676520632.
No sufficient data to compute Hardy-weinberg probability for ss3676520632.
There is no individual genotype data for ss3676520632.
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