Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000004.11:g.121809676C>G

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2504 sample genotypes.

Variant displays