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: 0.28 (G)
Location

Chromosome 10:99536106 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60151853, rs4442471

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

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2292 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays