Original source

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

Alleles
A/G|Ambiguity code: R|MAF: 0.46 (G)
Location

Chromosome 5:171391965 (forward strand)|View in location tab

Co-located variant

dbSNP rs200103231 (A/-/G/GG/GGG)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2506 sample genotypes.

Variant displays