Original source

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

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

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

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

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