Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.37 (A)
Location

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

Most severe consequence
Evidence status

Clinical significance

This variation has 2 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 2549 individual genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variation displays