Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.37 (C)

Chromosome 7:44163407 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61057400, rs17832276

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 4317 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays