Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 18:29172937 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM098273, CM870020, CM920684

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Variation displays