Original source

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

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

Chromosome 4:9782798 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000004.10:g.9393520C>T

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays