Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.02 (A)
Location

Chromosome 7:22821933 (forward strand)|View in location tab

Co-located variant

dbSNP rs201300337 (A/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs10349039

HGVS names

This variant has 7 HGVS names - Show

About this variant

Variant displays