Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 5:174156297 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001249

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_033_MSX2_123101_0003, 1400

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

Variation displays