Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.17 (G)
Location

Chromosome 6:161386823 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM032983

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 14 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2509 sample genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variant displays