Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M
Location

Chromosome 16:67809271 (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 24 transcripts and has 3 individual genotypes.

Variation displays