Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 2:232538854 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.232538854G>C

About this variant

This variant overlaps 7 transcripts and has 2 individual genotypes.

Variation displays