Submitter Handle ILLUMINA Submitter SNP ID Marazitafacialvariation_11779814_A_exm1242607-0_T_F_1921783333 RefSNP(rs#) clustering in process Submitted Batch ID OmniExpressExomeCustom_121313 Submitted Date Nov 14, 2018 Publication Cited N.D. First entry to dbSNP Nov 14 2018 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 968515 Population N.D. Allele Observed Allele G/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|ss3744944022|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic TGACTGATGG GCTGGTGGAG GGCGA S GCAGGCACCA GCAGCGAGAA GAACC   Submitted Frequency for ss3744944022 There is no frequency submission for ss3744944022.   dbSNP summary of Genotypes for ss3744944022 No sufficient data to compute Hardy-weinberg probability for ss3744944022.   Submitted individual genotype for ss3744944022 There is no individual genotype data for ss3744944022.

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