Original source

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

A/- | Ancestral: A | MAF: 0.46 (A)

Chromosome 5:126543263 (forward strand) | View in location tab


with dbSNP rs200532010 (A/C)

Most severe consequence
Evidence status

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

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 5 transcripts and has 1099 individual genotypes.

Variation displays