Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.11 (A)
Location

Chromosome 16:57541049 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.57541049C>A

About this variant

This variant overlaps 8 transcripts and has 2507 individual genotypes.

Variation displays