Original source

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

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

Chromosome 4:120888521 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


LSDB NC_000004.11:g.121809676C>G

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays