| Submitter | | Handle | ILLUMINA | | Submitter SNP ID | HumanOmniExpressExome-8v1-2_B_rs5110-131_B_F_1893184362 | | RefSNP(rs#) | clustering in process | | Submitted Batch ID | HumanOmniExpressExome-8v1-2_B | | Submitted Date | Dec 28, 2017 | | Publication Cited | N.D. | | First entry to dbSNP | Dec 28 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-CHIP | | Ascertainment Samplesize | 964193 | | Population | N.D. |
| | Allele | | Observed Allele | C/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|ss3640184699|allelePos=26|len=51|taxid=9606|alleles='C/A'|mol=Genomic GCACCTGCTC CTGCTGCTGC TCCTG
M
TGCTGTTCCT GCTGTTGCTC CAGCT
There is no frequency submission for ss3640184699.
No sufficient data to compute Hardy-weinberg probability for ss3640184699.
There is no individual genotype data for ss3640184699.
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