Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 6:49431354 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3205263

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1 sample genotype.

Variant displays