Original source

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

Alleles
-/GGT
Location

Chromosome 10: between 77982170 and 77982171 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB NM_007055.3:c.3742insACC, NM_007055.3:c.3742_3743insACC

This variation has 5 HGVS names - click the plus to show

Variation displays