Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 2:55865604 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.55865604C>G

About this variant

This variant overlaps 3 transcripts.

Variation displays