Original source

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

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

Chromosome 11:72243790 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013244

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_250_PHOX2A_602753_0003, 11442

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

Variation displays