Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

Chromosome 17:43115750 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM101974, CM041681

Most severe consequence
Clinical significance

Synonyms

LSDB U14680.1:c.110C>G, U14680.1:c.110C>A

This variation has 80 HGVS names - click the plus to show

Variation displays