Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 3:55313400 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

3:g.55313400A>C

This variation has assays on 10 chips - click the plus to show

Variation displays