Original source

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

Alleles
G/- | Ancestral: G
Location

Chromosome 9:37424864 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD992266

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_012203.1:c.103delG, PH2_3

This variation has 10 HGVS names - click the plus to show

Variation displays