Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.01 (A)
Location

Chromosome 19:33496679 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs253673, rs3826902

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2796 sample genotypes.

Variant displays