This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 CM961242, CM961243, CM020766

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

About this variant

This variant overlaps 18 transcripts, is associated with 6 phenotypes and is mentioned in 3 citations.

Variation displays