Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: < 0.01 (G)
Location

Chromosome 16:31188078 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs60903675

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 15 transcripts and has 2858 sample genotypes.

Variant displays