Submitter | Handle | ILLUMINA | Submitter SNP ID | OmniExpressExome-8v1-1_C_rs11596955-131_B_R_1891374154 | RefSNP(rs#) | clustering in process | Submitted Batch ID | HumanOmniExpressExome-8v1-1_C | Submitted Date | Jan 22, 2019 | Publication Cited | N.D. | First entry to dbSNP | Jan 22 2019 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-CHIP | Ascertainment Samplesize | 958178 | Population | N.D. |
| Allele | Observed Allele | A/C | 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|ss3772189987|allelePos=26|len=51|taxid=9606|alleles='A/C'|mol=Genomic AGAATACAAG CCAGTTATTT TATCA
M
ATGTTTCTCA ATTTGATTTT GTCTC
There is no frequency submission for ss3772189987.
No sufficient data to compute Hardy-weinberg probability for ss3772189987.
There is no individual genotype data for ss3772189987.
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