Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 5:151230967 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940871, CM940872, CM086829

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2264, NM_000171.3:c.896G>A, 2265, NM_000171.3:c.896G>T

This variation has 18 HGVS names - click the plus to show

Variation displays