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 3:93884869 (forward strand) | View in location tab

Co-located

with COSMIC COSM2828539 (G/A) ; HGMD-PUBLIC CM951056

Most severe consequence
Evidence status

Synonyms

LSDB PS-HY14

This variation has 5 HGVS names - click the plus to show

Variation displays