Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 1:209622597 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000001.9:g.207862565C>T

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 10 transcripts.

Variant displays