Original source

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

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

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

Most severe consequence
Splice region variant
Evidence status


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