Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.11 (T)
Location

Chromosome 16:50743391 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57304152

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 3723 sample genotypes and is mentioned in 1 citation.

Variant displays