Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 14:99682961 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.99682961A>G

About this variant

This variant overlaps 6 transcripts and has 2505 individual genotypes.

Variation displays