Original source

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

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

Chromosome 2:74831002 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.74831002A>C

About this variant

This variant overlaps 3 transcripts.

Variation displays