Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.38 (A)
Location

Chromosome 19:41350981 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 4 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 7 transcripts, 1 regulatory feature, has 3962 sample genotypes and is mentioned in 9 citations.

Variant displays