Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)

Chromosome 7:97022094 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs17271651, rs57723071

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 3908 sample genotypes and is mentioned in 1 citation.

Variant displays