Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanCoreExome-12v1-0_C_exm-rs41531144-132_T_R_1990486736 | RefSNP(rs#) | rs41531144 | Submitted Batch ID | HumanCoreExome12v10_c | Submitted Date | Oct 29, 2015 | Publication Cited | N.D. | First entry to dbSNP | Oct 29 2015 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 | T/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|ss1945966262|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic TACTTACTAA AGTGTGTTAA TTAAT
Y
AATGCTTGTA GGACATAATA ATAAC
There is no frequency submission for ss1945966262.
No sufficient data to compute Hardy-weinberg probability for ss1945966262.
There is no individual genotype data for ss1945966262.
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