Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 1:169530805 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001987

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 17290

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays