| 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 | 2536661 | Population | N.D. |
| Allele | Observed Allele | T/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. |
|
>gnl|dbSNP|ss2632465462|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic TAACTTGATA ATTTCTTCCC ATTCT
Y
GTGCAATAAA TTTCCTTCCT GATCA
There is no frequency submission for ss2632465462.
No sufficient data to compute Hardy-weinberg probability for ss2632465462.
There is no individual genotype data for ss2632465462.
|