Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.27 (G)

Chromosome 10:31381633 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 24 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 24 transcripts, has 1432 individual genotypes and is mentioned in 1 citation.

Variation displays