Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.08 (T)
Location

Chromosome 1:109568617 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17516999, rs60716285

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 3122 sample genotypes.

Variant displays