Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.30 (A)
Location

Chromosome 12:42459282 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 7 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 3765 individual genotypes and is mentioned in 1 citation.

Variation displays