Original source

Variants (including SNPs and indels) imported from dbSNP (release 136) | [View in dbSNP]

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

Chromosome 4:83029642 (forward strand) | View in location tab

Most severe consequence
HGVS name

4:g.83029642A>G

About this variant

This variant overlaps 2 transcripts.

Variation displays