Original source

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

Alleles
-/AAGACC/CA/CG
Location

Chromosome 7: between 101136457 and 101136458 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59199672

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays