Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)
Location

Chromosome 3:165772869 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.165772869C>A

About this variant

This variant overlaps 4 transcripts and has 1094 individual genotypes.

Variation displays