Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.10 (C)

Chromosome 11:7001129 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 5 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3978 sample genotypes.

Variant displays