Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 9:136677537 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020918

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_007_AGPAT2_603100_0001, 11640

This variation has 8 HGVS names - click the plus to show

Variation displays