Original source

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

Alleles
AA/-|MAF: 0.01 (-)
Location

Chromosome 7:101128962-101128963 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs376316305, rs201280512

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays