Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (T)

Chromosome 7:11563272 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61686367

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3748 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays