Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 12:120437215 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.120437215C>A

About this variant

This variant overlaps 4 transcripts and has 174 individual genotypes.

Variation displays