Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.07 (T)
Location

Chromosome 19:49907755 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3183979, rs3848552

HGVS names

This variant has 9 HGVS names - Show

About this variant

Variant displays