Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.03 (C)
Location

Chromosome 10:48404370 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2505 individual genotypes.

Variation displays