Original source

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

Alleles
T/-|Ancestral: T|MAF: 0.07 (T)
Location

Chromosome 16:79593778 (forward strand)|View in location tab

Co-located variant

dbSNP rs79761316 (T/A)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs35268223

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2506 sample genotypes.

Variant displays