Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 4:38797171 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM114630

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_003263.3:c.1661A>G

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is associated with 1 phenotype.

Variant displays