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 2:219253994 (forward strand) | View in location tab

Most severe consequence

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts and has 269 individual genotypes.

Variation displays