Original source

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

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

Chromosome 19:17877823 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981846

Most severe consequence
Clinical significance

Synonyms

LSDB 10648

This variation has 3 HGVS names - click the plus to show

19:g.17877823C>G
ENST00000222248.3:c.799C>G
ENSP00000222248.2:p.Gln267Glu

Variation displays