Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 3695 sample genotypes.

Variant displays