Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.38 (G)
Location

Chromosome 9:239313 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17719611, rs57869076

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 3120 sample genotypes.

Variant displays