Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 19:5831926 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3896734, rs2561800

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2506 sample genotypes.

Variant displays