Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.19 (A)
Location

Chromosome 4:3512359 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2600 individual genotypes.

Variation displays