Original source

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

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

Chromosome 8:22164263 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and is mentioned in 1 citation.

Variant displays