Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 12:56078510 (forward strand) | View in location tab

Most severe consequence
HGVS name

12:g.56078510G>A

About this variant

This variant overlaps 10 transcripts and has 1 individual genotype.

Variation displays