Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status


Archive dbSNP rs11552820, rs17354724

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 48 transcripts and has 2 individual genotypes.

Variation displays