Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 3:93877155 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM057362, CM991071

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4977, PS-HY22

This variation has 10 HGVS names - click the plus to show

Variation displays