Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.11 (G)
Location

Chromosome 1:97078702 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2506 individual genotypes and is mentioned in 1 citation.

Variation displays