Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)

Chromosome 15:73325378 (forward strand) | View in location tab


with HGMD-PUBLIC CM041785

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 13006, 2010_April_001_017_HCN4_605206_0003

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays