Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmni5-4v1_B_rs4433435-131_T_R_1893175600 | RefSNP(rs#) | rs4433435 | Submitted Batch ID | HumanOmni5-4v1_B | Submitted Date | Jun 22, 2012 | Publication Cited | N.D. | First entry to dbSNP | Jun 22 2012 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 | 2 | Population | N.D. |
| Allele | Observed Allele | G/C | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | SNV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss537235914|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic TCAAAATCTG GAGCAAATAG TAATC
S
TCTGTGTTGT TTTCCTACCA ACCCA
There is no frequency submission for ss537235914.
No sufficient data to compute Hardy-weinberg probability for ss537235914.
There is no individual genotype data for ss537235914.
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