Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.02 (G)
Location

Chromosome 12:55452754 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 5 transcripts and has 2775 individual genotypes.

Variation displays