Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 5:174729222 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930500

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1398, 2010_April_001_032_MSX2_123101_0001, NM_002449.4:c.443C>A

This variation has 4 HGVS names - click the plus to show

Variation displays