Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.07 (G)
Location

Chromosome 4:119164293 (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 7 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2310 individual genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variation displays