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 2:127421420 (forward strand) | View in location tab

Most severe consequence
Synonyms

LSDB PC-HY17

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts.

Variation displays