Original source

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

Alleles
-/GTAAGCTATTAAAAAAAGG/TAAGCTATTAAAAAAAGGG
Location

Chromosome 14: between 35402236 and 35402237 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs147444522

This variation has 16 HGVS names - click the plus to show

Variation displays