Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.30 (G)
Location

Chromosome 10:52773037 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60942321

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2665 individual genotypes and is mentioned in 1 citation.

Variation displays