Original source

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

Alleles
C/A/G|Ancestral: C|Ambiguity code: V
Location

Chromosome 8:22164057 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

Archive dbSNP rs11552820, rs17354724

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 48 transcripts and has 2 sample genotypes.

Variant displays