Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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