Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 19:40765266 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3199504

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 1 sample genotype.

Variant displays