Original source

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

Alleles
A/T|Ancestral: T|Ambiguity code: W|MAF: 0.18 (A)
Location

Chromosome 19:5832681 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61198699

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2514 sample genotypes.

Variant displays