Original source

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

Alleles
A/T|Ancestral: T|Ambiguity code: W|MAF: < 0.01 (A)
Location

Chromosome 9:136682936 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57373909

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays