Submitter | Handle | 1000G_HIGH_COVERAGE | Submitter SNP ID | chr8_31032012_G_A | RefSNP(rs#) | clustering in process | Submitted Batch ID | 30x_grch38_unfiltered | Submitted Date | Dec 09, 2021 | Publication Cited | N.D. | First entry to dbSNP | Dec 9 2021 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 | SEQ | Ascertainment Samplesize | 6404 | Population | 30x |
| 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|ss5566695291|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic AAGTCCCCTC TGGGAGTTCA AGCGG
R
TCATCGTCTC CACCTCTTCG TTCTT
There is no frequency submission for ss5566695291.
No sufficient data to compute Hardy-weinberg probability for ss5566695291.
There is no individual genotype data for ss5566695291.
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