Original source

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

Alleles
-/AT/TA
Location

Chromosome 7: between 97020190 and 97020191 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

About this variant

This variant overlaps 6 transcripts and has 6 individual genotypes.

Variation displays