Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/G
Location

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

Co-located

with dbSNP rs5886002 (A/C/G/T)

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 4 individual genotypes.

Variation displays