Original source

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

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

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