Original source

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

T/- | Ancestral: T | MAF: 0.37 (-)

Chromosome 10:112954192 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 1099 individual genotypes.

Variation displays