Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.35 (A)
Location

Chromosome 7:39460922 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386609852, rs17713083

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

About this variant

This variant overlaps 5 transcripts and has 3765 individual genotypes.

Variation displays