Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.49 (G)
Location

Chromosome 19:51008674 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17714889, rs74255838

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 4891 sample genotypes and is mentioned in 1 citation.

Variant displays