Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.03 (C)
Location

Chromosome 8:94249454 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61208598, rs17734556

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

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2506 sample genotypes.

Variant displays