Original source

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

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

Chromosome 17:41267767 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041681, CM101974

Most severe consequence
Clinical significance

Synonyms

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

This variation has 92 HGVS names - click the plus to show

Variation displays