Original source

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

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

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

Co-located variant

dbSNP rs370553515 (G/TC)

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays