Original source

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

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

Chromosome 19:8974071 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 1 transcript and has 2776 individual genotypes.

Variation displays