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 19:18705148 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030431

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_022_CRLF1_604237_0002, NM_004750.4:c.1121T>G

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

Variation displays