Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]


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


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

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 3 transcripts and has 5 individual genotypes.

Variation displays