Original source

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

Alleles
-/G/GG|MAF: 0.19 (-)
Location

Chromosome 19: between 16485848 and 16485849 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs376552064

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2510 sample genotypes.

Variant displays