Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: 0.01 (T)
Location

Chromosome 15:74720646 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM057662

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 6 synonyms - Show

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 20 transcripts, has 2888 sample genotypes and is mentioned in 17 citations.

Variant displays