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: < 0.01 (A)
Location

Chromosome 1:11022290 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM091849, CM081449

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 75 HGVS names - click the plus to show

About this variant

This variant overlaps 105 transcripts, has 2504 individual genotypes, is associated with 4 phenotypes and is mentioned in 2 citations.

Variation displays