Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 5:151855047 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012967

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2273, NM_000171.3:c.690C>A

This variation has 7 HGVS names - click the plus to show

Variation displays