Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.36 (A)

Chromosome 15:74041072 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61518227

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 16 transcripts, 1 regulatory feature, has 4325 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays