Submitter Handle CSHL Submitter SNP ID LID=SNVhg19:chr4:119220935 RefSNP(rs#) rs1490944020 Submitted Batch ID F23_WholeGenome_SNVs Submitted Date Oct 02, 2017 Publication Cited [1] DNA sequence level analysis reveals modifiers of phenotypic expression in a large family with psychiatric illness. First entry to dbSNP Oct 2 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 F23_WHOLE_GENOME_SEQUENCING Ascertainment Samplesize 96 Population Scotland Allele Observed Allele A/T 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|ss3345922021|allelePos=26|len=51|taxid=9606|alleles='A/T'|mol=Genomic TAAATAAAAT TAAATAAAAT AAAAT W AAATAAAATA AAATAAATAA AATAA   Submitted Frequency for ss3345922021 There is no frequency submission for ss3345922021.   dbSNP summary of Genotypes for ss3345922021 No sufficient data to compute Hardy-weinberg probability for ss3345922021.   Submitted individual genotype for ss3345922021 There is no individual genotype data for ss3345922021.

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