Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.29 (T)
Location

Chromosome 1:16996703 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60249437

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 14 transcripts, has 2782 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays