Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.40 (C)
Location

Chromosome 3:48294318 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and has 2510 sample genotypes.

Variant displays