Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 5:151268175 (forward strand) | View in location tab

Co-located

with dbSNP rs370553515 (G/TC)

Most severe consequence
 
3 prime UTR variant

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays