Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.11 (A)
Location

Chromosome 19:33495473 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs388725, rs253672, rs835582

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2774 sample genotypes.

Variant displays