Original source

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

Alleles
-/T|MAF: 0.47 (-)
Location

Chromosome 10: between 112951913 and 112951914 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs377427223, rs143225562

HGVS names

This variant has 16 HGVS names - Show

About this variant

Variant displays