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 5:151829060 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062763, CM950593

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000171.3:c.920A>C, NM_000171.3:c.920A>G, 2267

This variation has 12 HGVS names - click the plus to show

Variation displays