Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | 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 name

7:g.155465199A>G

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 3692 sample genotypes and is mentioned in 3 citations.

Variant displays