Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.29 (G)
Location

Chromosome 19:51888735 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17835331, rs57978823

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2579 sample genotypes.

Variant displays