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
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

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

About this variant

This variant overlaps 8 transcripts, has 3962 individual genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variation displays