Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 8:18063560 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs17126197, rs11538146

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2 sample genotypes.

Variant displays