Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 5:151230953 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970685

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2269, NM_000171.3:c.910A>G

This variation has 9 HGVS names - click the plus to show

Variation displays