Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.42 (G)
Location

Chromosome 19:42099624 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

Archive dbSNP rs58652270

This variant has 13 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 3724 sample genotypes and is mentioned in 1 citation.

Variant displays