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 9:129663881 (forward strand) | View in location tab

Most severe consequence
HGVS name

9:g.129663881G>A

About this variant

This variant overlaps 1 transcript.

Variation displays