Original source

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

Alleles
A/G/T|Ancestral: A|Ambiguity code: D|MAF: 0.29 (G)
Location

Chromosome 15:74719300 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR961724

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, has 2508 sample genotypes and is mentioned in 83 citations.

Variant displays