Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.31 (C)
Location

Chromosome 8:42537799 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs61116903

This variant has 9 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2511 sample genotypes.

Variant displays