Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.01 (-)
Location

Chromosome 5:132298019 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs374152861

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays