Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.16 (G)

Chromosome 7:155465199 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status


Archive dbSNP rs56669777, rs10356201

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3692 sample genotypes and is mentioned in 3 citations.

Variant displays