Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 12:6845700 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM117875

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 7 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 21 transcripts, has 3285 sample genotypes and is mentioned in 2 citations.

Variant displays