Original source

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

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

Chromosome 19:40232719 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs17366549

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 20 transcripts.

Variant displays