Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.16 (G)
Location

Chromosome 6:160718825 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2588 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays