Original source

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

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

Chromosome 18:31592975 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971538, CM920683

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4849, 4884

This variation has 24 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays