Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:18710530 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030430

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_004750.4:c.242G>A, 2010_April_001_023_CRLF1_604237_0002

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

Variation displays