Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: < 0.01 (C)
Location

Chromosome 10:87863158 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

Synonyms

ClinVar SCV000149471

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays