Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.33 (T)
Location

Chromosome 19:21096829 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56965544, rs4396644

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2779 sample genotypes.

Variant displays