Original source

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

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

Chromosome 4:52895950 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961272 ; PhenCode SGCB:c.323T>G (A/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_072_SGCB_600900_0006, 9621

This variation has 10 HGVS names - click the plus to show

Variation displays