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 8:132866134 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1235322

HGVS name

8:g.132866134G>A

About this variant

This variant overlaps 2 transcripts and has 2 individual genotypes.

Variation displays