Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.26 (G)
Location

Chromosome 10:99536106 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60151853, rs4442471

This variant has 3 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2506 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays