Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.33 (A)
Location

Chromosome 16:23182544 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR014917

Most severe consequence
Evidence status

HGVS name

16:g.23182544A>G

About this variant

This variant overlaps 2 transcripts, has 2507 individual genotypes and is mentioned in 1 citation.

Variation displays