Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/-|Ancestral: G
Location

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

Co-located variant

HGMD-PUBLIC CD992266

Most severe consequence
 
Frameshift variant
Evidence status

Clinical significance

Synonyms

LSDB NM_012203.1:c.103delG, PH2_3

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays