Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | View in dbSNP

G/C | Ambiguity code: S

Chromosome 18:73163 (forward strand) | View in location tab

Most severe consequence
Missense variant

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts.

Variant displays