Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanExome-12v1-1_B_exm7281-0_T_R_1921415516 | RefSNP(rs#) | rs116230480 | Submitted Batch ID | HumanExome-12v1-1 | Submitted Date | Oct 16, 2015 | Publication Cited | N.D. | First entry to dbSNP | Oct 16 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 |
| | 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|ss1917721638|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic ACTGGTTCCC ACCTTTCCAT CATAG
Y
TCCCAACTGC CAGGAACTGA CTGCT
There is no frequency submission for ss1917721638.
No sufficient data to compute Hardy-weinberg probability for ss1917721638.
There is no individual genotype data for ss1917721638.
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