Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.35 (G)
Location

Chromosome 4:6302228 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM021365

Most severe consequence
 
Missense variant
Evidence status

Synonyms
HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4066 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays