Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.50 (T)
Location

Chromosome 19:22051986 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs11669276

HGVS name

19:g.22051986T>G

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts and has 3695 sample genotypes.

Variant displays