Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 7:128250595 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61291665

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2773 sample genotypes.

Variant displays