Original source

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

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

Chromosome 3:171027031 (forward strand) | View in location tab

Most severe consequence
HGVS name

3:g.171027031A>G

About this variant

This variant overlaps 3 transcripts.

Variation displays