Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.22 (T)
Location

Chromosome 19:21114093 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4586578

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2509 sample genotypes.

Variant displays