Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2 sample genotypes.

Variant displays