Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.18 (G)
Location

Chromosome 18:31397165 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59778516, rs12968970

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2782 sample genotypes.

Variant displays