Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.41 (G)
Location

Chromosome 9:121321812 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs811112

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2509 sample genotypes.

Variant displays