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

Chromosome 10:43113621 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020766, CM961243, CM961242

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 39 HGVS names - click the plus to show

Variation displays