Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.17 (T)
Location

Chromosome 6:52425961 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3827792

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays