Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 17:80168330 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.80168330C>A

About this variant

This variant overlaps 6 transcripts and has 2505 individual genotypes.

Variation displays