Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 4:73982136 (forward strand) | View in location tab

Most severe consequence
HGVS name

4:g.73982136G>A

About this variant

This variant overlaps 3 transcripts and has 269 individual genotypes.

Variation displays