Original source

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

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

Chromosome 11:68448857 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB LRP5_4635C_T_112410

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays