Original source

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

Alleles
-/C
Location

Chromosome 16: between 67806324 and 67806325 (forward strand) | View in location tab

Most severe consequence

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts.

Variation displays