Submitter Handle BIOINF_KMB_FNS_UNIBA Submitter SNP ID 11.112155192T>C RefSNP(rs#) rs4988359 Submitted Batch ID Horsa 1.0 Submitted Date Jul 05, 2017 Publication Cited [1] Non invasive prenatal testing is a valuable source of population specific allelic frequencies First entry to dbSNP Jul 5 2017 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 LOWCOVERAGENGS Ascertainment Samplesize 1548 Population N.D. Allele Observed Allele T/C Ancestral Allele N.D. Allele Origin N/A SNP Class SNV CpG Code N.D. Validation Validation Status Not Validated HWE Goodness of Fit not applicable Homozygote Detected PCR Confirmed In Expressed Sequence Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss3027254983|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic ATGAACAATC TTGACATTCA ATAAA Y GCCAGAAGTT TCAGCTTATG AATAC   Submitted Frequency for ss3027254983 There is no frequency submission for ss3027254983.   dbSNP summary of Genotypes for ss3027254983 No sufficient data to compute Hardy-weinberg probability for ss3027254983.   Submitted individual genotype for ss3027254983 There is no individual genotype data for ss3027254983.

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