Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.12 (C)
Location

Chromosome 3:190388453 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60307624

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2626 individual genotypes.

Variation displays