Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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