Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.33 (C)
Location

Chromosome 10:69462737 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17569148

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

About this variant

This variant overlaps 6 transcripts and has 2565 sample genotypes.

Variant displays