Submitter | Handle | LUNTER | Submitter SNP ID | CEU_3_37822802-37822803 | RefSNP(rs#) | rs59945410 | Submitted Batch ID | indel_calls_from_1000_genomes_pilot_1_CEU | Submitted Date | Nov 21, 2012 | Publication Cited | [1] The Origin, evolution and functional impact of short insertion-deletion variants identified in 179 human genomes | First entry to dbSNP | Nov 21 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 |
| | Allele | Observed Allele | GT/- | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | 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|ss551224567|allelePos=26|len=51|taxid=9606|alleles='GT/-'|mol=Genomic TGGGTGTGTG TGTGTGTGCG TGCGC
N
GTGTGTGTGT GTATGTGACT TCCTT
There is no frequency submission for ss551224567.
No sufficient data to compute Hardy-weinberg probability for ss551224567.
There is no individual genotype data for ss551224567.
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