Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.09 (A)
Location

Chromosome 10:6011200 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 1652 individual genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variation displays