Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.02 (A)
Location

Chromosome 2:192749169 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.192749169C>A

About this variant

This variant overlaps 2 transcripts and has 2772 individual genotypes.

Variation displays