Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanCNV370v1_C_rs1544198 | RefSNP(rs#) | rs1544198 | Submitted Batch ID | HumanCNV370v1 | Submitted Date | Apr 14, 2009 | Publication Cited | N.D. | First entry to dbSNP | Apr 14 2009 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 | INFINIUM-II | Ascertainment Samplesize | 270 | Population | N.D. |
| Allele | Observed Allele | C/T | 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|ss121744626|allelePos=61|len=121|taxid=9606|alleles='C/T'|mol=Genomic TTGGAACGAT CACCTTCACT AGACAGCCTG GAGTCAAGGG AGGGACACAG GAGACCATTA
Y
CTGCAAGTCC TAAGGGACAG AAGGGACATT TATCATCTCC CAGCACTGCC TTCATCAGCC
There is no frequency submission for ss121744626.
No sufficient data to compute Hardy-weinberg probability for ss121744626.
There is no individual genotype data for ss121744626.
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