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 2:192747872 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.192747872A>G

About this variant

This variant overlaps 2 transcripts and has 2504 individual genotypes.

Variation displays