Original source

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

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

Most severe consequence
 
Intron variant
Evidence status

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2506 sample genotypes.

Variant displays