This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.09 (A)
Location

Chromosome 13:113118845 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940396, CM074160

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays