Original source

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

Alleles
T/A/G | Ancestral: T | Ambiguity code: D
Location

Chromosome 18:31595152 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910376, CM890113

Most severe consequence
Clinical significance

Synonyms

LSDB 4854, 4838

This variation has 16 HGVS names - click the plus to show

Variation displays