Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 4:102885221 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS075098

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001008388.1:c.109G>C, 17053

This variation has 9 HGVS names - click the plus to show

Variation displays