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: 0.04 (G)
Location

Chromosome 12:40278187 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2142 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays