Original source

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

Alleles
-/G
Location

Chromosome 7: between 97020572 and 97020573 (forward strand)|View in location tab

Co-located variant

dbSNP rs5886002 (A/C/G/T)

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 4 sample genotypes.

Variant displays