Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.39 (A)
Location

Chromosome 1:17010896 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 3693 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays