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
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.14 (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 6 chips - click the plus to show

About this variant

This variant overlaps 36 transcripts, has 4283 individual genotypes, is associated with 2 phenotypes and is mentioned in 23 citations.

Variation displays