Simple Nucleotide Polymorphisms (dbSNP 150) Found in >= 1% of Samples
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dbSNP build 150 rs2076658
dbSNP: rs2076658
Position: chr1:11194951-11194951
Band: 1p36.22
Genomic Size: 1
View DNA for this feature (hg38/Human)
Summary: C>C/T (chimp allele displayed first, then '>', then human alleles)
Strand: +
Observed: C/T
Class | single |
Validation | by-cluster,by-frequency,by-submitter,by-2hit-2allele,by-hapmap,by-1000genomes |
Function | synonymous_variant, intron_variant, nc_transcript_variant |
Molecule Type | genomic |
Average Heterozygosity | 0.108 +/- 0.206 |
Weight | 1 |
Submitter Handles | 1000GENOMES, BGI, CLINSEQ_SNP, COMPLETE_GENOMICS, DDI, EGP_SNPS, EVA-GONL, EVA_DECODE, EVA_EXAC, EVA_FINRISK, EVA_MGP, EVA_SVP, EVA_UK10K_ALSPAC, EVA_UK10K_TWINSUK, GENOMED, GMI, HAMMER_LAB, HGBASE, HUMAN_LONGEVITY, ILLUMINA, JJLAB, JMKIDD_LAB, KRIBB_YJKIM, NHLBI-ESP, PERLEGEN, SEATTLESEQ, SSMP, TISHKOFF, TOPMED, USC_VALOUEV, WEILL_CORNELL_DGM, YUSUKE |
Allele Frequencies | C: 5.906% (7453 / 126202); T: 94.094% (118749 / 126202) |
Miscellaneous properties annotated by dbSNP:
Minor Allele Frequency is at least 5% in at least one population assayed
Coding annotations by dbSNP:
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