This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N
Location

Chromosome 19:41848120 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041083, CM041084

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

Variation displays