Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 1:77926761 (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 15 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 3825 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays